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rs796053019

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053019(C;G)
Make rs796053019(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165996065
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053019
ebirs796053019
HLIrs796053019
Exacrs796053019
Varsomers796053019
Maprs796053019
PheGenIrs796053019
hapmaprs796053019
1000 genomesrs796053019
hgdprs796053019
ensemblrs796053019
gopubmedrs796053019
geneviewrs796053019
scholarrs796053019
googlers796053019
pharmgkbrs796053019
gwascentralrs796053019
openSNPrs796053019
23andMers796053019
23andMe allrs796053019
SNP Nexus

SNPshotrs796053019
SNPdbers796053019
MSV3drs796053019
GWAS Ctlgrs796053019
Max Magnitude0
ClinVar
Risk rs796053019(G;G)
Alt rs796053019(G;G)
Reference rs796053019(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166852575G>C
CLNSRC
CLNACC RCV000188959.1,