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rs796053129

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053129(A;A)
Make rs796053129(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165373319
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053129
ebirs796053129
HLIrs796053129
Exacrs796053129
Varsomers796053129
Maprs796053129
PheGenIrs796053129
hapmaprs796053129
1000 genomesrs796053129
hgdprs796053129
ensemblrs796053129
gopubmedrs796053129
geneviewrs796053129
scholarrs796053129
googlers796053129
pharmgkbrs796053129
gwascentralrs796053129
openSNPrs796053129
23andMers796053129
23andMe allrs796053129
SNP Nexus

SNPshotrs796053129
SNPdbers796053129
MSV3drs796053129
GWAS Ctlgrs796053129
Max Magnitude0
ClinVar
Risk rs796053129(A;A)
Alt rs796053129(A;A)
Reference rs796053129(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166229829G>A
CLNSRC
CLNACC RCV000189140.2,