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rs796053198

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053198(-;-)
Make rs796053198(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165310333
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053198
ebirs796053198
HLIrs796053198
Exacrs796053198
Varsomers796053198
Maprs796053198
PheGenIrs796053198
hapmaprs796053198
1000 genomesrs796053198
hgdprs796053198
ensemblrs796053198
gopubmedrs796053198
geneviewrs796053198
scholarrs796053198
googlers796053198
pharmgkbrs796053198
gwascentralrs796053198
openSNPrs796053198
23andMers796053198
23andMe allrs796053198
SNP Nexus

SNPshotrs796053198
SNPdbers796053198
MSV3drs796053198
GWAS Ctlgrs796053198
Max Magnitude0
ClinVar
Risk rs796053198(;)
Alt rs796053198(;)
Reference rs796053198(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166166843delC
CLNSRC
CLNACC RCV000189236.1,