Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894171
rs104894171
MINPP1
G 0.800 CausalMutation CLINVAR

dbSNP: rs114817817
rs114817817
SRGAP1 ; LOC105369798
T 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs11554290
rs11554290
NRAS
C 0.800 CausalMutation CLINVAR

dbSNP: rs119486096
rs119486096
MINPP1 ; LOC112268064
T 0.800 CausalMutation CLINVAR

dbSNP: rs28933406
rs28933406
HRAS ; LRRC56
T 0.800 CausalMutation CLINVAR

dbSNP: rs781626187
rs781626187
SRGAP1 ; LOC105369801
C 0.800 CausalMutation CLINVAR

dbSNP: rs797044990
rs797044990
SRGAP1
A 0.800 CausalMutation CLINVAR

dbSNP: rs104894228
rs104894228
HRAS ; LRRC56
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894229
rs104894229
HRAS ; LRRC56
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894230
rs104894230
HRAS ; LRRC56
G 0.700 CausalMutation CLINVAR

dbSNP: rs121913364
rs121913364
BRAF
C 0.700 CausalMutation CLINVAR

dbSNP: rs1564566774
rs1564566774
PTEN
T 0.700 CausalMutation CLINVAR