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rs796053072

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053072(-;-)
Make rs796053072(-;AT)
Make rs796053072(AT;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166012262
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053072
ebirs796053072
HLIrs796053072
Exacrs796053072
Varsomers796053072
Maprs796053072
PheGenIrs796053072
hapmaprs796053072
1000 genomesrs796053072
hgdprs796053072
ensemblrs796053072
gopubmedrs796053072
geneviewrs796053072
scholarrs796053072
googlers796053072
pharmgkbrs796053072
gwascentralrs796053072
openSNPrs796053072
23andMers796053072
23andMe allrs796053072
SNP Nexus

SNPshotrs796053072
SNPdbers796053072
MSV3drs796053072
GWAS Ctlgrs796053072
Max Magnitude0
ClinVar
Risk rs796053072(AT;AT)
Alt rs796053072(AT;AT)
Reference rs796053072(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166868773_166868774dupAT
CLNSRC
CLNACC RCV000189052.1,