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rs796053086

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053086(-;-)
Make rs796053086(-;ATCA)
Make rs796053086(ATCA;ATCA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991563
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053086
ebirs796053086
HLIrs796053086
Exacrs796053086
Varsomers796053086
Maprs796053086
PheGenIrs796053086
hapmaprs796053086
1000 genomesrs796053086
hgdprs796053086
ensemblrs796053086
gopubmedrs796053086
geneviewrs796053086
scholarrs796053086
googlers796053086
pharmgkbrs796053086
gwascentralrs796053086
openSNPrs796053086
23andMers796053086
23andMe allrs796053086
SNP Nexus

SNPshotrs796053086
SNPdbers796053086
MSV3drs796053086
GWAS Ctlgrs796053086
Max Magnitude0
ClinVar
Risk rs796053086(ATCA;ATCA)
Alt rs796053086(ATCA;ATCA)
Reference rs796053086(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848074_166848077dupTGAT
CLNSRC
CLNACC RCV000189068.1,