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rs796052995

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052995(C;T)
Make rs796052995(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166013842
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796052995
ebirs796052995
HLIrs796052995
Exacrs796052995
Varsomers796052995
Maprs796052995
PheGenIrs796052995
hapmaprs796052995
1000 genomesrs796052995
hgdprs796052995
ensemblrs796052995
gopubmedrs796052995
geneviewrs796052995
scholarrs796052995
googlers796052995
pharmgkbrs796052995
gwascentralrs796052995
openSNPrs796052995
23andMers796052995
23andMe allrs796052995
SNP Nexus

SNPshotrs796052995
SNPdbers796052995
MSV3drs796052995
GWAS Ctlgrs796052995
Max Magnitude0
ClinVar
Risk rs796052995(T;T)
Alt rs796052995(T;T)
Reference rs796052995(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166870352G>A
CLNSRC
CLNACC RCV000188920.1,