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rs796053067

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053067(-;-)
Make rs796053067(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166036483
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053067
ebirs796053067
HLIrs796053067
Exacrs796053067
Varsomers796053067
Maprs796053067
PheGenIrs796053067
hapmaprs796053067
1000 genomesrs796053067
hgdprs796053067
ensemblrs796053067
gopubmedrs796053067
geneviewrs796053067
scholarrs796053067
googlers796053067
pharmgkbrs796053067
gwascentralrs796053067
openSNPrs796053067
23andMers796053067
23andMe allrs796053067
SNP Nexus

SNPshotrs796053067
SNPdbers796053067
MSV3drs796053067
GWAS Ctlgrs796053067
Max Magnitude0
ClinVar
Risk rs796053067(;)
Alt rs796053067(;)
Reference rs796053067(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166892993delG
CLNSRC
CLNACC RCV000189047.1,