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rs41311087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41311087(C;T)
Make rs41311087(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38633255
GeneSCN5A
is asnp
is mentioned by
dbSNPrs41311087
ebirs41311087
HLIrs41311087
Exacrs41311087
Varsomers41311087
Maprs41311087
PheGenIrs41311087
hapmaprs41311087
1000 genomesrs41311087
hgdprs41311087
ensemblrs41311087
gopubmedrs41311087
geneviewrs41311087
scholarrs41311087
googlers41311087
pharmgkbrs41311087
gwascentralrs41311087
openSNPrs41311087
23andMers41311087
23andMe allrs41311087
SNP Nexus

SNPshotrs41311087
SNPdbers41311087
MSV3drs41311087
GWAS Ctlgrs41311087
Max Magnitude0
ClinVar
Risk rs41311087(T;T)
Alt rs41311087(T;T)
Reference rs41311087(C;C)
Significance Pathogenic
Disease not specified Brugada syndrome
Variation info
Gene SCN5A
CLNDBN not specified Brugada syndrome
Reversed 0
HGVS NC_000003.11:g.38674746C>T
CLNSRC ClinVar
CLNACC RCV000041626.3, RCV000058779.2,