GH1, growth hormone 1, 2688

N. diseases: 686; N. variants: 27
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853220
rs137853220
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C1849779
Disease:
Kowarski syndrome
0.800 GeneticVariation UNIPROT Evaluation of the biological activity of a growth hormone (GH) mutant (R77C) and its impact on GH responsiveness and stature. 17519310 2007
dbSNP: rs137853221
rs137853221
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C1849779
Disease:
Kowarski syndrome
0.800 GeneticVariation UNIPROT Evaluation of the biological activity of a growth hormone (GH) mutant (R77C) and its impact on GH responsiveness and stature. 17519310 2007
dbSNP: rs137853223
rs137853223
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C0271567
Disease:
Isolated Growth Hormone Deficiency, Type II
0.800 GeneticVariation UNIPROT Autosomal dominant GH deficiency due to an Arg183His GH-1 gene mutation: clinical and molecular evidence of impaired regulated GH secretion. 11502836 2001
dbSNP: rs137853220
rs137853220
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C1849779
Disease:
Kowarski syndrome
0.800 GeneticVariation UNIPROT Biologically inactive growth hormone caused by an amino acid substitution. 9276733 1997
dbSNP: rs137853221
rs137853221
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C1849779
Disease:
Kowarski syndrome
0.800 GeneticVariation UNIPROT Biologically inactive growth hormone caused by an amino acid substitution. 9276733 1997
dbSNP: rs137853223
rs137853223
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C0271567
Disease:
Isolated Growth Hormone Deficiency, Type II
0.800 GeneticVariation UNIPROT Detection of growth hormone gene defects by dideoxy fingerprinting (ddF). 9152628 1997
dbSNP: rs137853220
rs137853220
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C1849779
Disease:
Kowarski syndrome
0.800 GeneticVariation UNIPROT Brief report: short stature caused by a mutant growth hormone. 8552145 1996
dbSNP: rs137853221
rs137853221
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C1849779
Disease:
Kowarski syndrome
0.800 GeneticVariation UNIPROT Brief report: short stature caused by a mutant growth hormone. 8552145 1996
dbSNP: rs137853220
rs137853220
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C1849779
Disease:
Kowarski syndrome
A 0.800 CausalMutation CLINVAR
dbSNP: rs137853221
rs137853221
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C1849779
Disease:
Kowarski syndrome
C 0.800 CausalMutation CLINVAR
dbSNP: rs137853223
rs137853223
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C0271567
Disease:
Isolated Growth Hormone Deficiency, Type II
T 0.800 CausalMutation CLINVAR
dbSNP: rs2005172
rs2005172
Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0424678
Disease:
Lean body mass
0.700 GeneticVariation GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698 2019
dbSNP: rs137853219
rs137853219
Entrez Id: 1444;2688
Gene Symbol: CSHL1;GH1
CSHL1;GH1
CUI: C0342573
Disease:
PITUITARY DWARFISM I
T 0.700 CausalMutation CLINVAR
dbSNP: rs137853222
rs137853222
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C1849779
Disease:
Kowarski syndrome
G 0.700 CausalMutation CLINVAR
dbSNP: rs71640273
rs71640273
Entrez Id: 1444;2688
Gene Symbol: CSHL1;GH1
CSHL1;GH1
CUI: C2748571
Disease:
Isolated Growth Hormone Deficiency, Type IB
0.700 GeneticVariation UNIPROT
dbSNP: rs71640276
rs71640276
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C2748571
Disease:
Isolated Growth Hormone Deficiency, Type IB
0.700 GeneticVariation UNIPROT
dbSNP: rs71640277
rs71640277
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C0271567
Disease:
Isolated Growth Hormone Deficiency, Type II
G 0.700 CausalMutation CLINVAR
dbSNP: rs71640277
rs71640277
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C0271567
Disease:
Isolated Growth Hormone Deficiency, Type II
T 0.700 CausalMutation CLINVAR
dbSNP: rs797044449
rs797044449
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C4722273
Disease:
ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV
G 0.700 CausalMutation CLINVAR
dbSNP: rs797044449
rs797044449
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C4722273
Disease:
ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV
A 0.700 CausalMutation CLINVAR
dbSNP: rs797044450
rs797044450
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C0271567
Disease:
Isolated Growth Hormone Deficiency, Type II
G 0.700 CausalMutation CLINVAR
dbSNP: rs863223306
rs863223306
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C0271567
Disease:
Isolated Growth Hormone Deficiency, Type II
T 0.700 CausalMutation CLINVAR
dbSNP: rs863223307
rs863223307
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C0271567
Disease:
Isolated Growth Hormone Deficiency, Type II
T 0.700 CausalMutation CLINVAR
dbSNP: rs863223308
rs863223308
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C4722273
Disease:
ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV
G 0.700 CausalMutation CLINVAR
dbSNP: rs863223309
rs863223309
Entrez Id: 1444;2688;112268204
Gene Symbol: CSHL1;GH1;LOC112268204
CSHL1;GH1;LOC112268204
CUI: C0271567
Disease:
Isolated Growth Hormone Deficiency, Type II
A 0.700 CausalMutation CLINVAR