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rs775026107

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs775026107(C;C)
Make rs775026107(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38554338
GeneSCN5A
is asnp
is mentioned by
dbSNPrs775026107
ebirs775026107
HLIrs775026107
Exacrs775026107
Varsomers775026107
Maprs775026107
PheGenIrs775026107
hapmaprs775026107
1000 genomesrs775026107
hgdprs775026107
ensemblrs775026107
gopubmedrs775026107
geneviewrs775026107
scholarrs775026107
googlers775026107
pharmgkbrs775026107
gwascentralrs775026107
openSNPrs775026107
23andMers775026107
23andMe allrs775026107
SNP Nexus

SNPshotrs775026107
SNPdbers775026107
MSV3drs775026107
GWAS Ctlgrs775026107
Max Magnitude0
ClinVar
Risk rs775026107(C;C)
Alt rs775026107(C;C)
Reference rs775026107(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38595829T>C
CLNSRC
CLNACC RCV000183083.1,