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rs796053000

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053000(A;A)
Make rs796053000(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166012164
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053000
ebirs796053000
HLIrs796053000
Exacrs796053000
Varsomers796053000
Maprs796053000
PheGenIrs796053000
hapmaprs796053000
1000 genomesrs796053000
hgdprs796053000
ensemblrs796053000
gopubmedrs796053000
geneviewrs796053000
scholarrs796053000
googlers796053000
pharmgkbrs796053000
gwascentralrs796053000
openSNPrs796053000
23andMers796053000
23andMe allrs796053000
SNP Nexus

SNPshotrs796053000
SNPdbers796053000
MSV3drs796053000
GWAS Ctlgrs796053000
Max Magnitude0
ClinVar
Risk rs796053000(A;A)
Alt rs796053000(A;A)
Reference rs796053000(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166868674C>T
CLNSRC
CLNACC RCV000188931.1,