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rs796053055

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053055(-;-)
Make rs796053055(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166046955
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053055
ebirs796053055
HLIrs796053055
Exacrs796053055
Varsomers796053055
Maprs796053055
PheGenIrs796053055
hapmaprs796053055
1000 genomesrs796053055
hgdprs796053055
ensemblrs796053055
gopubmedrs796053055
geneviewrs796053055
scholarrs796053055
googlers796053055
pharmgkbrs796053055
gwascentralrs796053055
openSNPrs796053055
23andMers796053055
23andMe allrs796053055
SNP Nexus

SNPshotrs796053055
SNPdbers796053055
MSV3drs796053055
GWAS Ctlgrs796053055
Max Magnitude0
ClinVar
Risk rs796053055(;)
Alt rs796053055(;)
Reference rs796053055(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166903465delT
CLNSRC
CLNACC RCV000189035.1,