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rs796053192

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053192(-;-)
Make rs796053192(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165365144
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053192
ebirs796053192
HLIrs796053192
Exacrs796053192
Varsomers796053192
Maprs796053192
PheGenIrs796053192
hapmaprs796053192
1000 genomesrs796053192
hgdprs796053192
ensemblrs796053192
gopubmedrs796053192
geneviewrs796053192
scholarrs796053192
googlers796053192
pharmgkbrs796053192
gwascentralrs796053192
openSNPrs796053192
23andMers796053192
23andMe allrs796053192
SNP Nexus

SNPshotrs796053192
SNPdbers796053192
MSV3drs796053192
GWAS Ctlgrs796053192
Max Magnitude0
ClinVar
Risk rs796053192(;)
Alt rs796053192(;)
Reference rs796053192(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166221654delA
CLNSRC
CLNACC RCV000189230.1,