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

rs757843082

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs757843082(C;C)
Make rs757843082(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38557260
GeneSCN5A
is asnp
is mentioned by
dbSNPrs757843082
ebirs757843082
HLIrs757843082
Exacrs757843082
Varsomers757843082
Maprs757843082
PheGenIrs757843082
hapmaprs757843082
1000 genomesrs757843082
hgdprs757843082
ensemblrs757843082
gopubmedrs757843082
geneviewrs757843082
scholarrs757843082
googlers757843082
pharmgkbrs757843082
gwascentralrs757843082
openSNPrs757843082
23andMers757843082
23andMe allrs757843082
SNP Nexus

SNPshotrs757843082
SNPdbers757843082
MSV3drs757843082
GWAS Ctlgrs757843082
Max Magnitude0
ClinVar
Risk rs757843082(A,C;A,C)
Alt rs757843082(A,C;A,C)
Reference rs757843082(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38598751T>A
CLNSRC
CLNACC RCV000183068.2,