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rs796053017

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053017(A;A)
Make rs796053017(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165996101
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053017
ebirs796053017
HLIrs796053017
Exacrs796053017
Varsomers796053017
Maprs796053017
PheGenIrs796053017
hapmaprs796053017
1000 genomesrs796053017
hgdprs796053017
ensemblrs796053017
gopubmedrs796053017
geneviewrs796053017
scholarrs796053017
googlers796053017
pharmgkbrs796053017
gwascentralrs796053017
openSNPrs796053017
23andMers796053017
23andMe allrs796053017
SNP Nexus

SNPshotrs796053017
SNPdbers796053017
MSV3drs796053017
GWAS Ctlgrs796053017
Max Magnitude0
ClinVar
Risk rs796053017(A;A)
Alt rs796053017(A;A)
Reference rs796053017(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166852611A>T
CLNSRC
CLNACC RCV000188957.1,