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rs796053066

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053066(-;-)
Make rs796053066(-;TAT)
Make rs796053066(TAT;TAT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166041306
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053066
ebirs796053066
HLIrs796053066
Exacrs796053066
Varsomers796053066
Maprs796053066
PheGenIrs796053066
hapmaprs796053066
1000 genomesrs796053066
hgdprs796053066
ensemblrs796053066
gopubmedrs796053066
geneviewrs796053066
scholarrs796053066
googlers796053066
pharmgkbrs796053066
gwascentralrs796053066
openSNPrs796053066
23andMers796053066
23andMe allrs796053066
SNP Nexus

SNPshotrs796053066
SNPdbers796053066
MSV3drs796053066
GWAS Ctlgrs796053066
Max Magnitude0
ClinVar
Risk rs796053066(TAT;TAT)
Alt rs796053066(TAT;TAT)
Reference rs796053066(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166897816_166897817insATA
CLNSRC
CLNACC RCV000189046.1,