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rs750013499

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs750013499(A;G)
Make rs750013499(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38551345
GeneSCN5A
is asnp
is mentioned by
dbSNPrs750013499
ebirs750013499
HLIrs750013499
Exacrs750013499
Varsomers750013499
Maprs750013499
PheGenIrs750013499
hapmaprs750013499
1000 genomesrs750013499
hgdprs750013499
ensemblrs750013499
gopubmedrs750013499
geneviewrs750013499
scholarrs750013499
googlers750013499
pharmgkbrs750013499
gwascentralrs750013499
openSNPrs750013499
23andMers750013499
23andMe allrs750013499
SNP Nexus

SNPshotrs750013499
SNPdbers750013499
MSV3drs750013499
GWAS Ctlgrs750013499
Max Magnitude0
ClinVar
Risk rs750013499(G;G)
Alt rs750013499(G;G)
Reference rs750013499(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38592836A>G
CLNSRC
CLNACC RCV000183097.1,