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rs199473190

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473190(A;A)
Make rs199473190(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38579474
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473190
ebirs199473190
HLIrs199473190
Exacrs199473190
Varsomers199473190
Maprs199473190
PheGenIrs199473190
hapmaprs199473190
1000 genomesrs199473190
hgdprs199473190
ensemblrs199473190
gopubmedrs199473190
geneviewrs199473190
scholarrs199473190
googlers199473190
pharmgkbrs199473190
gwascentralrs199473190
openSNPrs199473190
23andMers199473190
23andMe allrs199473190
SNP Nexus

SNPshotrs199473190
SNPdbers199473190
MSV3drs199473190
GWAS Ctlgrs199473190
Max Magnitude0
ClinVar
Risk rs199473190(A,C;A,C)
Alt rs199473190(A,C;A,C)
Reference rs199473190(G;G)
Significance Pathogenic
Disease not specified SUDDEN INFANT DEATH SYNDROME
Variation info
Gene SCN5A
CLNDBN not specified SUDDEN INFANT DEATH SYNDROME
Reversed 1
HGVS NC_000003.11:g.38620965C>G; NC_000003.11:g.38620965C>T
CLNSRC ClinVar
CLNACC RCV000156018.1, RCV000058558.2,