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rs763880032

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs763880032(C;T)
Make rs763880032(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38551187
GeneSCN5A
is asnp
is mentioned by
dbSNPrs763880032
ebirs763880032
HLIrs763880032
Exacrs763880032
Varsomers763880032
Maprs763880032
PheGenIrs763880032
hapmaprs763880032
1000 genomesrs763880032
hgdprs763880032
ensemblrs763880032
gopubmedrs763880032
geneviewrs763880032
scholarrs763880032
googlers763880032
pharmgkbrs763880032
gwascentralrs763880032
openSNPrs763880032
23andMers763880032
23andMe allrs763880032
SNP Nexus

SNPshotrs763880032
SNPdbers763880032
MSV3drs763880032
GWAS Ctlgrs763880032
Max Magnitude0
ClinVar
Risk rs763880032(T;T)
Alt rs763880032(T;T)
Reference rs763880032(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38592678C>T
CLNSRC
CLNACC RCV000183107.1,