Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434482
rs121434482
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
G 0.800 CausalMutation CLINVAR
dbSNP: rs121434485
rs121434485
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
C 0.800 CausalMutation CLINVAR
dbSNP: rs121434486
rs121434486
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
C 0.800 CausalMutation CLINVAR
dbSNP: rs121434487
rs121434487
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
A 0.800 CausalMutation CLINVAR
dbSNP: rs121434490
rs121434490
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
C 0.800 CausalMutation CLINVAR
dbSNP: rs121434488
rs121434488
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C1848201
Disease:
Subcortical Band Heterotopia
C 0.710 CausalMutation CLINVAR
dbSNP: rs1057520515
rs1057520515
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
A 0.700 CausalMutation CLINVAR
dbSNP: rs113994198
rs113994198
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
GA 0.700 CausalMutation CLINVAR
dbSNP: rs113994200
rs113994200
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
TG 0.700 CausalMutation CLINVAR
dbSNP: rs113994200
rs113994200
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
T 0.700 CausalMutation CLINVAR
dbSNP: rs113994202
rs113994202
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
C 0.700 CausalMutation CLINVAR
dbSNP: rs113994203
rs113994203
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
A 0.700 CausalMutation CLINVAR
dbSNP: rs121434483
rs121434483
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
T 0.700 CausalMutation CLINVAR
dbSNP: rs121434484
rs121434484
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C1848201
Disease:
Subcortical Band Heterotopia
C 0.700 CausalMutation CLINVAR
dbSNP: rs121434489
rs121434489
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C1848201
Disease:
Subcortical Band Heterotopia
T 0.700 CausalMutation CLINVAR
dbSNP: rs121434489
rs121434489
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
T 0.700 CausalMutation CLINVAR
dbSNP: rs1555526309
rs1555526309
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555526718
rs1555526718
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
TA 0.700 CausalMutation CLINVAR
dbSNP: rs1555526733
rs1555526733
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555527149
rs1555527149
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555527743
rs1555527743
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
T 0.700 CausalMutation CLINVAR
dbSNP: rs1567559851
rs1567559851
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
A 0.700 CausalMutation CLINVAR
dbSNP: rs1567561137
rs1567561137
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
G 0.700 CausalMutation CLINVAR
dbSNP: rs200390886
rs200390886
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
A 0.700 GeneticVariation CLINVAR
dbSNP: rs369259961
rs369259961
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
G 0.700 CausalMutation CLINVAR