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rs796053052

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053052(-;-)
Make rs796053052(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166058585
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053052
ebirs796053052
HLIrs796053052
Exacrs796053052
Varsomers796053052
Maprs796053052
PheGenIrs796053052
hapmaprs796053052
1000 genomesrs796053052
hgdprs796053052
ensemblrs796053052
gopubmedrs796053052
geneviewrs796053052
scholarrs796053052
googlers796053052
pharmgkbrs796053052
gwascentralrs796053052
openSNPrs796053052
23andMers796053052
23andMe allrs796053052
SNP Nexus

SNPshotrs796053052
SNPdbers796053052
MSV3drs796053052
GWAS Ctlgrs796053052
Max Magnitude0
ClinVar
Risk rs796053052(;)
Alt rs796053052(;)
Reference rs796053052(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166915095delT
CLNSRC
CLNACC RCV000189032.1,