Have questions? Visit https://www.reddit.com/r/SNPedia

rs786204839

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204839(A;A)
Make rs786204839(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38605949
GeneSCN5A
is asnp
is mentioned by
dbSNPrs786204839
ebirs786204839
HLIrs786204839
Exacrs786204839
Varsomers786204839
Maprs786204839
PheGenIrs786204839
hapmaprs786204839
1000 genomesrs786204839
hgdprs786204839
ensemblrs786204839
gopubmedrs786204839
geneviewrs786204839
scholarrs786204839
googlers786204839
pharmgkbrs786204839
gwascentralrs786204839
openSNPrs786204839
23andMers786204839
23andMe allrs786204839
SNP Nexus

SNPshotrs786204839
SNPdbers786204839
MSV3drs786204839
GWAS Ctlgrs786204839
Max Magnitude0
ClinVar
Risk rs786204839(A;A)
Alt rs786204839(A;A)
Reference rs786204839(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38647440A>T
CLNSRC
CLNACC RCV000169744.2,