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rs796053080

From SNPedia

Orientationminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs796053080(-;-)
Make rs796053080(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165994220
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053080
ebirs796053080
HLIrs796053080
Exacrs796053080
Varsomers796053080
Maprs796053080
PheGenIrs796053080
hapmaprs796053080
1000 genomesrs796053080
hgdprs796053080
ensemblrs796053080
gopubmedrs796053080
geneviewrs796053080
scholarrs796053080
googlers796053080
pharmgkbrs796053080
gwascentralrs796053080
openSNPrs796053080
23andMers796053080
23andMe allrs796053080
SNP Nexus

SNPshotrs796053080
SNPdbers796053080
MSV3drs796053080
GWAS Ctlgrs796053080
Max Magnitude0
ClinVar
Risk rs796053080(;)
Alt rs796053080(;)
Reference rs796053080(AT;AT)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166850730_166850731delAT
CLNSRC
CLNACC RCV000189060.1,