Gene: SPTBN2 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918306
rs121918306
SPTBN2
G 0.840 CausalMutation CLINVAR

dbSNP: rs397514749
rs397514749
SPTBN2
A 0.800 CausalMutation CLINVAR

dbSNP: rs1554984881
rs1554984881
SPTBN2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554986337
rs1554986337
SPTBN2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs875989881
rs875989881
SPTBN2
G 0.700 GeneticVariation CLINVAR