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rs796053053

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053053(-;-)
Make rs796053053(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166054764
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053053
ebirs796053053
HLIrs796053053
Exacrs796053053
Varsomers796053053
Maprs796053053
PheGenIrs796053053
hapmaprs796053053
1000 genomesrs796053053
hgdprs796053053
ensemblrs796053053
gopubmedrs796053053
geneviewrs796053053
scholarrs796053053
googlers796053053
pharmgkbrs796053053
gwascentralrs796053053
openSNPrs796053053
23andMers796053053
23andMe allrs796053053
SNP Nexus

SNPshotrs796053053
SNPdbers796053053
MSV3drs796053053
GWAS Ctlgrs796053053
Max Magnitude0
ClinVar
Risk rs796053053(;)
Alt rs796053053(;)
Reference rs796053053(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166911274delT
CLNSRC
CLNACC RCV000189033.1,