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rs796052987

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052987(G;G)
Make rs796052987(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166037921
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052987
ebirs796052987
HLIrs796052987
Exacrs796052987
Varsomers796052987
Maprs796052987
PheGenIrs796052987
hapmaprs796052987
1000 genomesrs796052987
hgdprs796052987
ensemblrs796052987
gopubmedrs796052987
geneviewrs796052987
scholarrs796052987
googlers796052987
pharmgkbrs796052987
gwascentralrs796052987
openSNPrs796052987
23andMers796052987
23andMe allrs796052987
SNP Nexus

SNPshotrs796052987
SNPdbers796052987
MSV3drs796052987
GWAS Ctlgrs796052987
Max Magnitude0
ClinVar
Risk rs796052987(G;G)
Alt rs796052987(G;G)
Reference rs796052987(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894431A>C
CLNSRC
CLNACC RCV000188899.1,