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rs796053074

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053074(-;-)
Make rs796053074(-;T)
Make rs796053074(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166012134
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053074
ebirs796053074
HLIrs796053074
Exacrs796053074
Varsomers796053074
Maprs796053074
PheGenIrs796053074
hapmaprs796053074
1000 genomesrs796053074
hgdprs796053074
ensemblrs796053074
gopubmedrs796053074
geneviewrs796053074
scholarrs796053074
googlers796053074
pharmgkbrs796053074
gwascentralrs796053074
openSNPrs796053074
23andMers796053074
23andMe allrs796053074
SNP Nexus

SNPshotrs796053074
SNPdbers796053074
MSV3drs796053074
GWAS Ctlgrs796053074
Max Magnitude0
ClinVar
Risk rs796053074(T;T)
Alt rs796053074(T;T)
Reference rs796053074(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166868645dupA
CLNSRC
CLNACC RCV000189054.1,