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

rs373172185

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs373172185(A;G)
Make rs373172185(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38606675
GeneSCN5A
is asnp
is mentioned by
dbSNPrs373172185
ebirs373172185
HLIrs373172185
Exacrs373172185
Varsomers373172185
Maprs373172185
PheGenIrs373172185
hapmaprs373172185
1000 genomesrs373172185
hgdprs373172185
ensemblrs373172185
gopubmedrs373172185
geneviewrs373172185
scholarrs373172185
googlers373172185
pharmgkbrs373172185
gwascentralrs373172185
openSNPrs373172185
23andMers373172185
23andMe allrs373172185
SNP Nexus

SNPshotrs373172185
SNPdbers373172185
MSV3drs373172185
GWAS Ctlgrs373172185
Max Magnitude0
ClinVar
Risk rs373172185(G;G)
Alt rs373172185(G;G)
Reference rs373172185(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38648166A>T
CLNSRC
CLNACC RCV000182961.1,