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rs778522112

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs778522112(A;A)
Make rs778522112(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38603722
GeneSCN5A
is asnp
is mentioned by
dbSNPrs778522112
ebirs778522112
HLIrs778522112
Exacrs778522112
Varsomers778522112
Maprs778522112
PheGenIrs778522112
hapmaprs778522112
1000 genomesrs778522112
hgdprs778522112
ensemblrs778522112
gopubmedrs778522112
geneviewrs778522112
scholarrs778522112
googlers778522112
pharmgkbrs778522112
gwascentralrs778522112
openSNPrs778522112
23andMers778522112
23andMe allrs778522112
SNP Nexus

SNPshotrs778522112
SNPdbers778522112
MSV3drs778522112
GWAS Ctlgrs778522112
Max Magnitude0
ClinVar
Risk rs778522112(A;A)
Alt rs778522112(A;A)
Reference rs778522112(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene SCN5A
CLNDBN not provided not specified
Reversed 0
HGVS NC_000003.11:g.38645213G>A
CLNSRC
CLNACC RCV000183173.2, RCV000223692.1,