Gene: HEXB ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1007338250
rs1007338250
HEXB
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060499701
rs1060499701
HEXB
C 0.700 CausalMutation CLINVAR

dbSNP: rs1114167287
rs1114167287
HEXB
A 0.700 CausalMutation CLINVAR

dbSNP: rs138914144
rs138914144
HEXB
T 0.700 CausalMutation CLINVAR

dbSNP: rs1453919511
rs1453919511
HEXB
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554034423
rs1554034423
HEXB
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554034447
rs1554034447
HEXB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554034449
rs1554034449
HEXB
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554034505
rs1554034505
HEXB
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554036523
rs1554036523
HEXB
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554036638
rs1554036638
HEXB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554037076
rs1554037076
HEXB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554037120
rs1554037120
HEXB
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554037129
rs1554037129
HEXB
CAGAG 0.700 GeneticVariation CLINVAR

dbSNP: rs1554037137
rs1554037137
HEXB ; GFM2
CCTATGACAGACTGACA 0.700 GeneticVariation CLINVAR

dbSNP: rs1554037170
rs1554037170
HEXB ; GFM2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs398123443
rs398123443
HEXB
A 0.700 CausalMutation CLINVAR

dbSNP: rs398123446
rs398123446
HEXB
G 0.700 GeneticVariation CLINVAR

dbSNP: rs5030731
rs5030731
HEXB
A 0.700 CausalMutation CLINVAR

dbSNP: rs761197472
rs761197472
HEXB
C 0.700 CausalMutation CLINVAR

dbSNP: rs768438206
rs768438206
HEXB
A 0.700 CausalMutation CLINVAR

dbSNP: rs776476415
rs776476415
HEXB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs886039499
rs886039499
HEXB
A 0.700 GeneticVariation CLINVAR

dbSNP: rs892920643
rs892920643
HEXB
A 0.700 GeneticVariation CLINVAR

dbSNP: rs967720287
rs967720287
HEXB
A 0.700 GeneticVariation CLINVAR