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rs796053178

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053178(C;G)
Make rs796053178(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165313732
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053178
ebirs796053178
HLIrs796053178
Exacrs796053178
Varsomers796053178
Maprs796053178
PheGenIrs796053178
hapmaprs796053178
1000 genomesrs796053178
hgdprs796053178
ensemblrs796053178
gopubmedrs796053178
geneviewrs796053178
scholarrs796053178
googlers796053178
pharmgkbrs796053178
gwascentralrs796053178
openSNPrs796053178
23andMers796053178
23andMe allrs796053178
SNP Nexus

SNPshotrs796053178
SNPdbers796053178
MSV3drs796053178
GWAS Ctlgrs796053178
Max Magnitude0
ClinVar
Risk rs796053178(G;G)
Alt rs796053178(G;G)
Reference rs796053178(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166170242C>G
CLNSRC
CLNACC RCV000189204.2,