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rs796053169

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053169(A;G)
Make rs796053169(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165307846
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053169
ebirs796053169
HLIrs796053169
Exacrs796053169
Varsomers796053169
Maprs796053169
PheGenIrs796053169
hapmaprs796053169
1000 genomesrs796053169
hgdprs796053169
ensemblrs796053169
gopubmedrs796053169
geneviewrs796053169
scholarrs796053169
googlers796053169
pharmgkbrs796053169
gwascentralrs796053169
openSNPrs796053169
23andMers796053169
23andMe allrs796053169
SNP Nexus

SNPshotrs796053169
SNPdbers796053169
MSV3drs796053169
GWAS Ctlgrs796053169
Max Magnitude0
ClinVar
Risk rs796053169(G;G)
Alt rs796053169(G;G)
Reference rs796053169(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166164356A>G
CLNSRC
CLNACC RCV000189190.2,