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rs756474485

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756474485(C;T)
Make rs756474485(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38598948
GeneSCN5A
is asnp
is mentioned by
dbSNPrs756474485
ebirs756474485
HLIrs756474485
Exacrs756474485
Varsomers756474485
Maprs756474485
PheGenIrs756474485
hapmaprs756474485
1000 genomesrs756474485
hgdprs756474485
ensemblrs756474485
gopubmedrs756474485
geneviewrs756474485
scholarrs756474485
googlers756474485
pharmgkbrs756474485
gwascentralrs756474485
openSNPrs756474485
23andMers756474485
23andMe allrs756474485
SNP Nexus

SNPshotrs756474485
SNPdbers756474485
MSV3drs756474485
GWAS Ctlgrs756474485
Max Magnitude0
ClinVar
Risk rs756474485(A,T;A,T)
Alt rs756474485(A,T;A,T)
Reference rs756474485(C;C)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene SCN5A
CLNDBN not provided not specified
Reversed 0
HGVS NC_000003.11:g.38640439C>A; NC_000003.11:g.38640439C>T
CLNSRC
CLNACC RCV000182993.2, RCV000223785.1, RCV000183175.2,