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rs1057517817

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517817(A;A)
Make rs1057517817(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position38562470
GeneSCN5A
is asnp
is mentioned by
dbSNPrs1057517817
dbSNP (old)rs1057517817
ClinGenrs1057517817
ebirs1057517817
HLIrs1057517817
Exacrs1057517817
Gnomadrs1057517817
Varsomers1057517817
Maprs1057517817
PheGenIrs1057517817
Biobankrs1057517817
1000 genomesrs1057517817
hgdprs1057517817
ensemblrs1057517817
gopubmedrs1057517817
geneviewrs1057517817
scholarrs1057517817
googlers1057517817
pharmgkbrs1057517817
gwascentralrs1057517817
openSNPrs1057517817
23andMers1057517817
23andMe allrs1057517817
SNPshotrs1057517817
SNPdbers1057517817
MSV3drs1057517817
GWAS Ctlgrs1057517817
Max Magnitude0
ClinVar
Risk rs1057517817(A;A)
Alt rs1057517817(A;A)
Reference Rs1057517817(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38603961C>T
CLNSRC
CLNACC RCV000413785.1,