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rs755767610

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755767610(G;T)
Make rs755767610(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38604018
GeneSCN5A
is asnp
is mentioned by
dbSNPrs755767610
ebirs755767610
HLIrs755767610
Exacrs755767610
Varsomers755767610
Maprs755767610
PheGenIrs755767610
hapmaprs755767610
1000 genomesrs755767610
hgdprs755767610
ensemblrs755767610
gopubmedrs755767610
geneviewrs755767610
scholarrs755767610
googlers755767610
pharmgkbrs755767610
gwascentralrs755767610
openSNPrs755767610
23andMers755767610
23andMe allrs755767610
SNP Nexus

SNPshotrs755767610
SNPdbers755767610
MSV3drs755767610
GWAS Ctlgrs755767610
Max Magnitude0
ClinVar
Risk rs755767610(T;T)
Alt rs755767610(T;T)
Reference rs755767610(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38645509G>T
CLNSRC
CLNACC RCV000182978.1,