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rs796053196

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053196(-;-)
Make rs796053196(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165307886
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053196
ebirs796053196
HLIrs796053196
Exacrs796053196
Varsomers796053196
Maprs796053196
PheGenIrs796053196
hapmaprs796053196
1000 genomesrs796053196
hgdprs796053196
ensemblrs796053196
gopubmedrs796053196
geneviewrs796053196
scholarrs796053196
googlers796053196
pharmgkbrs796053196
gwascentralrs796053196
openSNPrs796053196
23andMers796053196
23andMe allrs796053196
SNP Nexus

SNPshotrs796053196
SNPdbers796053196
MSV3drs796053196
GWAS Ctlgrs796053196
Max Magnitude0
ClinVar
Risk rs796053196(;)
Alt rs796053196(;)
Reference rs796053196(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166164396delA
CLNSRC
CLNACC RCV000189234.1,