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rs796053193

From SNPedia

Orientationplus
Geno Mag Summary
(TTA;TTA) 0 common in clinvar
Make rs796053193(-;-)
Make rs796053193(-;ATT)
Make rs796053193(ATT;ATT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165380655
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053193
ebirs796053193
HLIrs796053193
Exacrs796053193
Varsomers796053193
Maprs796053193
PheGenIrs796053193
hapmaprs796053193
1000 genomesrs796053193
hgdprs796053193
ensemblrs796053193
gopubmedrs796053193
geneviewrs796053193
scholarrs796053193
googlers796053193
pharmgkbrs796053193
gwascentralrs796053193
openSNPrs796053193
23andMers796053193
23andMe allrs796053193
SNP Nexus

SNPshotrs796053193
SNPdbers796053193
MSV3drs796053193
GWAS Ctlgrs796053193
Max Magnitude0
ClinVar
Risk rs796053193(;)
Alt rs796053193(;)
Reference rs796053193(TTA;TTA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166237165_166237167delATT
CLNSRC
CLNACC RCV000189231.1,