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rs796053183

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053183(A;C)
Make rs796053183(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165314014
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053183
ebirs796053183
HLIrs796053183
Exacrs796053183
Varsomers796053183
Maprs796053183
PheGenIrs796053183
hapmaprs796053183
1000 genomesrs796053183
hgdprs796053183
ensemblrs796053183
gopubmedrs796053183
geneviewrs796053183
scholarrs796053183
googlers796053183
pharmgkbrs796053183
gwascentralrs796053183
openSNPrs796053183
23andMers796053183
23andMe allrs796053183
SNP Nexus

SNPshotrs796053183
SNPdbers796053183
MSV3drs796053183
GWAS Ctlgrs796053183
Max Magnitude0
ClinVar
Risk rs796053183(C;C) rs796053183(G;G)
Alt rs796053183(C;C) rs796053183(G;G)
Reference Rs796053183(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166170524A>C; NC_000002.11:g.166170524A>G
CLNSRC
CLNACC RCV000189209.2, RCV000189210.2,