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rs796053016

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053016(C;G)
Make rs796053016(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166073379
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053016
ebirs796053016
HLIrs796053016
Exacrs796053016
Varsomers796053016
Maprs796053016
PheGenIrs796053016
hapmaprs796053016
1000 genomesrs796053016
hgdprs796053016
ensemblrs796053016
gopubmedrs796053016
geneviewrs796053016
scholarrs796053016
googlers796053016
pharmgkbrs796053016
gwascentralrs796053016
openSNPrs796053016
23andMers796053016
23andMe allrs796053016
SNP Nexus

SNPshotrs796053016
SNPdbers796053016
MSV3drs796053016
GWAS Ctlgrs796053016
Max Magnitude0
ClinVar
Risk rs796053016(G;G)
Alt rs796053016(G;G)
Reference rs796053016(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166929889G>C
CLNSRC
CLNACC RCV000188955.1,