Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518799
rs1057518799
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1837084
Disease:
Short metacarpal
TGATTGGCA 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518799
rs1057518799
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C0020676
Disease:
Hypothyroidism
TGATTGGCA 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518799
rs1057518799
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C0027092
Disease:
Myopia
TGATTGGCA 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518799
rs1057518799
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1384666
Disease:
hearing impairment
TGATTGGCA 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518799
rs1057518799
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C0349588
Disease:
Short stature
TGATTGGCA 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518799
rs1057518799
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1843367
Disease:
Poor school performance
TGATTGGCA 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518799
rs1057518799
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C4551560
Disease:
Truncal obesity
TGATTGGCA 0.700 GeneticVariation CLINVAR
dbSNP: rs1057519392
rs1057519392
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1843367
Disease:
Poor school performance
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057519392
rs1057519392
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C4225351
Disease:
White Sutton syndrome
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1131692270
rs1131692270
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C0454644
Disease:
Delayed speech and language development
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1131692270
rs1131692270
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C4225351
Disease:
White Sutton syndrome
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1135401798
rs1135401798
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C4225351
Disease:
White Sutton syndrome
A 0.700 CausalMutation CLINVAR
dbSNP: rs1276388879
rs1276388879
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1510586
Disease:
Autism Spectrum Disorders
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1372713010
rs1372713010
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1510586
Disease:
Autism Spectrum Disorders
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1418634444
rs1418634444
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1510586
Disease:
Autism Spectrum Disorders
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1452048149
rs1452048149
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1510586
Disease:
Autism Spectrum Disorders
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1476293577
rs1476293577
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1510586
Disease:
Autism Spectrum Disorders
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1484207450
rs1484207450
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1510586
Disease:
Autism Spectrum Disorders
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1553212374
rs1553212374
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C4225351
Disease:
White Sutton syndrome
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1553212868
rs1553212868
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1854882
Disease:
Absent speech
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553212868
rs1553212868
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C0020534
Disease:
Orbital separation excessive
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553212868
rs1553212868
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C1858120
Disease:
Generalized hypotonia
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553212868
rs1553212868
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C0221356
Disease:
Brachycephaly
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553212868
rs1553212868
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C0038379
Disease:
Strabismus
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553212868
rs1553212868
Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C0853087
Disease:
Nail abnormality
C 0.700 CausalMutation CLINVAR