Gene: EFNB1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894796
rs104894796
EFNB1
T 0.800 CausalMutation CLINVAR

dbSNP: rs104894801
rs104894801
EFNB1
T 0.800 CausalMutation CLINVAR

dbSNP: rs28935170
rs28935170
EFNB1
T 0.800 CausalMutation CLINVAR

dbSNP: rs28936069
rs28936069
EFNB1
A 0.800 CausalMutation CLINVAR

dbSNP: rs28936070
rs28936070
EFNB1
T 0.800 CausalMutation CLINVAR

dbSNP: rs28936071
rs28936071
EFNB1
G 0.800 CausalMutation CLINVAR

dbSNP: rs104894802
rs104894802
EFNB1
G 0.700 CausalMutation CLINVAR

dbSNP: rs104894803
rs104894803
EFNB1
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894804
rs104894804
EFNB1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057519033
rs1057519033
EFNB1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519034
rs1057519034
EFNB1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519035
rs1057519035
EFNB1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1556096780
rs1556096780
EFNB1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1556105849
rs1556105849
EFNB1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1556107481
rs1556107481
EFNB1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1556107856
rs1556107856
EFNB1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1556107925
rs1556107925
EFNB1
A 0.700 CausalMutation CLINVAR

dbSNP: rs587777109
rs587777109
EFNB1
T 0.700 CausalMutation CLINVAR