Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13135934
rs13135934
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1
CUI: C1314691
Disease:
Age at menarche 		C 0.700 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870 2014
dbSNP: rs1057519613
rs1057519613
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1
CUI: C1852150
Disease:
Fingerprints, Absence of 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1057519613
rs1057519613
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1
CUI: C1852150
Disease:
Fingerprints, Absence of 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1057519613
rs1057519613
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1
CUI: C0406707
Disease:
Basan syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1114167276
rs1114167276
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1
CUI: C1852150
Disease:
Fingerprints, Absence of 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1114167276
rs1114167276
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1
CUI: C0406767
Disease:
Keratoderma with scleroatrophy of the extremities 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1114167277
rs1114167277
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1
CUI: C1852150
Disease:
Fingerprints, Absence of 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1560542180
rs1560542180
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1
CUI: C0406767
Disease:
Keratoderma with scleroatrophy of the extremities 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1560542214
rs1560542214
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1
CUI: C0406767
Disease:
Keratoderma with scleroatrophy of the extremities 		GT 0.700 CausalMutation CLINVAR
dbSNP: rs895436485
rs895436485
Entrez Id: 56916
Gene Symbol: SMARCAD1
SMARCAD1
CUI: C0406707
Disease:
Basan syndrome 		T 0.700 CausalMutation CLINVAR