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rs796053085

From SNPedia

Orientationminus
Geno Mag Summary
(ACCCA;ACCCA) 0 common in clinvar
Make rs796053085(-;-)
Make rs796053085(-;ACCCA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991998
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053085
ebirs796053085
HLIrs796053085
Exacrs796053085
Varsomers796053085
Maprs796053085
PheGenIrs796053085
hapmaprs796053085
1000 genomesrs796053085
hgdprs796053085
ensemblrs796053085
gopubmedrs796053085
geneviewrs796053085
scholarrs796053085
googlers796053085
pharmgkbrs796053085
gwascentralrs796053085
openSNPrs796053085
23andMers796053085
23andMe allrs796053085
SNP Nexus

SNPshotrs796053085
SNPdbers796053085
MSV3drs796053085
GWAS Ctlgrs796053085
Max Magnitude0
ClinVar
Risk rs796053085(;)
Alt rs796053085(;)
Reference rs796053085(ACCCA;ACCCA)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848508_166848512delTGGGT
CLNSRC
CLNACC RCV000189066.1,