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rs796053139

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053139(C;C)
Make rs796053139(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165377652
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053139
ebirs796053139
HLIrs796053139
Exacrs796053139
Varsomers796053139
Maprs796053139
PheGenIrs796053139
hapmaprs796053139
1000 genomesrs796053139
hgdprs796053139
ensemblrs796053139
gopubmedrs796053139
geneviewrs796053139
scholarrs796053139
googlers796053139
pharmgkbrs796053139
gwascentralrs796053139
openSNPrs796053139
23andMers796053139
23andMe allrs796053139
SNP Nexus

SNPshotrs796053139
SNPdbers796053139
MSV3drs796053139
GWAS Ctlgrs796053139
Max Magnitude0
ClinVar
Risk rs796053139(C;C)
Alt rs796053139(C;C)
Reference rs796053139(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166234162T>C
CLNSRC
CLNACC RCV000189152.1,