Have questions? Visit https://www.reddit.com/r/SNPedia

rs796053128

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053128(C;T)
Make rs796053128(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165365177
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053128
ebirs796053128
HLIrs796053128
Exacrs796053128
Varsomers796053128
Maprs796053128
PheGenIrs796053128
hapmaprs796053128
1000 genomesrs796053128
hgdprs796053128
ensemblrs796053128
gopubmedrs796053128
geneviewrs796053128
scholarrs796053128
googlers796053128
pharmgkbrs796053128
gwascentralrs796053128
openSNPrs796053128
23andMers796053128
23andMe allrs796053128
SNP Nexus

SNPshotrs796053128
SNPdbers796053128
MSV3drs796053128
GWAS Ctlgrs796053128
Max Magnitude0
ClinVar
Risk rs796053128(T;T)
Alt rs796053128(T;T)
Reference rs796053128(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166221687C>T
CLNSRC
CLNACC RCV000189135.1,