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rs796053038

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053038(G;T)
Make rs796053038(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991914
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053038
ebirs796053038
HLIrs796053038
Exacrs796053038
Varsomers796053038
Maprs796053038
PheGenIrs796053038
hapmaprs796053038
1000 genomesrs796053038
hgdprs796053038
ensemblrs796053038
gopubmedrs796053038
geneviewrs796053038
scholarrs796053038
googlers796053038
pharmgkbrs796053038
gwascentralrs796053038
openSNPrs796053038
23andMers796053038
23andMe allrs796053038
SNP Nexus

SNPshotrs796053038
SNPdbers796053038
MSV3drs796053038
GWAS Ctlgrs796053038
Max Magnitude0
ClinVar
Risk rs796053038(T;T)
Alt rs796053038(T;T)
Reference rs796053038(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848424C>A
CLNSRC
CLNACC RCV000189001.2,