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rs796053073

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053073(-;-)
Make rs796053073(-;T)
Make rs796053073(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166012211
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053073
ebirs796053073
HLIrs796053073
Exacrs796053073
Varsomers796053073
Maprs796053073
PheGenIrs796053073
hapmaprs796053073
1000 genomesrs796053073
hgdprs796053073
ensemblrs796053073
gopubmedrs796053073
geneviewrs796053073
scholarrs796053073
googlers796053073
pharmgkbrs796053073
gwascentralrs796053073
openSNPrs796053073
23andMers796053073
23andMe allrs796053073
SNP Nexus

SNPshotrs796053073
SNPdbers796053073
MSV3drs796053073
GWAS Ctlgrs796053073
Max Magnitude0
ClinVar
Risk rs796053073(T;T)
Alt rs796053073(T;T)
Reference rs796053073(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166868722dupA
CLNSRC
CLNACC RCV000189053.1,