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rs796053012

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053012(A;A)
Make rs796053012(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165998154
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053012
ebirs796053012
HLIrs796053012
Exacrs796053012
Varsomers796053012
Maprs796053012
PheGenIrs796053012
hapmaprs796053012
1000 genomesrs796053012
hgdprs796053012
ensemblrs796053012
gopubmedrs796053012
geneviewrs796053012
scholarrs796053012
googlers796053012
pharmgkbrs796053012
gwascentralrs796053012
openSNPrs796053012
23andMers796053012
23andMe allrs796053012
SNP Nexus

SNPshotrs796053012
SNPdbers796053012
MSV3drs796053012
GWAS Ctlgrs796053012
Max Magnitude0
ClinVar
Risk rs796053012(A;A)
Alt rs796053012(A;A)
Reference rs796053012(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166854664C>T
CLNSRC
CLNACC RCV000188950.1,