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rs766751878

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs766751878(C;C)
Make rs766751878(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38550632
GeneSCN5A
is asnp
is mentioned by
dbSNPrs766751878
ebirs766751878
HLIrs766751878
Exacrs766751878
Varsomers766751878
Maprs766751878
PheGenIrs766751878
hapmaprs766751878
1000 genomesrs766751878
hgdprs766751878
ensemblrs766751878
gopubmedrs766751878
geneviewrs766751878
scholarrs766751878
googlers766751878
pharmgkbrs766751878
gwascentralrs766751878
openSNPrs766751878
23andMers766751878
23andMe allrs766751878
SNP Nexus

SNPshotrs766751878
SNPdbers766751878
MSV3drs766751878
GWAS Ctlgrs766751878
Max Magnitude0
ClinVar
Risk rs766751878(C;C)
Alt rs766751878(C;C)
Reference rs766751878(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38592123T>C
CLNSRC
CLNACC RCV000183132.1,