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rs796053076

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053076(-;-)
Make rs796053076(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166073481
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053076
ebirs796053076
HLIrs796053076
Exacrs796053076
Varsomers796053076
Maprs796053076
PheGenIrs796053076
hapmaprs796053076
1000 genomesrs796053076
hgdprs796053076
ensemblrs796053076
gopubmedrs796053076
geneviewrs796053076
scholarrs796053076
googlers796053076
pharmgkbrs796053076
gwascentralrs796053076
openSNPrs796053076
23andMers796053076
23andMe allrs796053076
SNP Nexus

SNPshotrs796053076
SNPdbers796053076
MSV3drs796053076
GWAS Ctlgrs796053076
Max Magnitude0
ClinVar
Risk rs796053076(;)
Alt rs796053076(;)
Reference rs796053076(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166929991delA
CLNSRC
CLNACC RCV000189056.1,