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

rs869025523

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025523(-;-)
Make rs869025523(-;TG)
Make rs869025523(TG;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position38597813
GeneSCN5A
is asnp
is mentioned by
dbSNPrs869025523
ebirs869025523
HLIrs869025523
Exacrs869025523
Varsomers869025523
Maprs869025523
PheGenIrs869025523
hapmaprs869025523
1000 genomesrs869025523
hgdprs869025523
ensemblrs869025523
gopubmedrs869025523
geneviewrs869025523
scholarrs869025523
googlers869025523
pharmgkbrs869025523
gwascentralrs869025523
openSNPrs869025523
23andMers869025523
23andMe allrs869025523
SNP Nexus

SNPshotrs869025523
SNPdbers869025523
MSV3drs869025523
GWAS Ctlgrs869025523
Max Magnitude0
ClinVar
Risk rs869025523(TG;TG)
Alt rs869025523(TG;TG)
Reference rs869025523(;)
Significance Probable-Pathogenic
Disease Left ventricular noncompaction cardiomyopathy
Variation info
Gene SCN5A
CLNDBN Left ventricular noncompaction cardiomyopathy
Reversed 1
HGVS NC_000003.11:g.38639305_38639306dupCA
CLNSRC
CLNACC RCV000208394.1,