Gene: HEXA ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519466
rs1057519466
HEXA
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121907965
rs121907965
HEXA ; HEXA-AS1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs121907969
rs121907969
HEXA
C 0.700 CausalMutation CLINVAR

dbSNP: rs121907980
rs121907980
HEXA
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1309204908
rs1309204908
HEXA
A 0.700 GeneticVariation CLINVAR

dbSNP: rs147324677
rs147324677
HEXA
A 0.700 GeneticVariation CLINVAR

dbSNP: rs150675340
rs150675340
HEXA
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555472262
rs1555472262
HEXA
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555472270
rs1555472270
HEXA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555472296
rs1555472296
HEXA
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555472432
rs1555472432
HEXA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555472440
rs1555472440
HEXA
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555472553
rs1555472553
HEXA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555473070
rs1555473070
HEXA
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555475498
rs1555475498
HEXA ; HEXA-AS1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555475519
rs1555475519
HEXA ; HEXA-AS1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1567295184
rs1567295184
HEXA
C 0.700 CausalMutation CLINVAR

dbSNP: rs267606862
rs267606862
HEXA
T 0.700 CausalMutation CLINVAR

dbSNP: rs387906949
rs387906949
HEXA ; HEXA-AS1
T 0.700 CausalMutation CLINVAR

dbSNP: rs543071358
rs543071358
HEXA
G 0.700 GeneticVariation CLINVAR

dbSNP: rs556872918
rs556872918
HEXA ; HEXA-AS1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs587779406
rs587779406
HEXA
A 0.700 CausalMutation CLINVAR

dbSNP: rs587779407
rs587779407
HEXA
TA 0.700 CausalMutation CLINVAR

dbSNP: rs751248523
rs751248523
HEXA
C 0.700 CausalMutation CLINVAR

dbSNP: rs751393950
rs751393950
HEXA ; HEXA-AS1
A 0.700 GeneticVariation CLINVAR