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rs796053107

From SNPedia

Orientationminus
Geno Mag Summary
(ACCTCTAAGAG;ACCTCTAAGAG) 0 common in clinvar
Make rs796053107(-;-)
Make rs796053107(-;ACCTCTAAGAG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166009745
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053107
ebirs796053107
HLIrs796053107
Exacrs796053107
Varsomers796053107
Maprs796053107
PheGenIrs796053107
hapmaprs796053107
1000 genomesrs796053107
hgdprs796053107
ensemblrs796053107
gopubmedrs796053107
geneviewrs796053107
scholarrs796053107
googlers796053107
pharmgkbrs796053107
gwascentralrs796053107
openSNPrs796053107
23andMers796053107
23andMe allrs796053107
SNP Nexus

SNPshotrs796053107
SNPdbers796053107
MSV3drs796053107
GWAS Ctlgrs796053107
Max Magnitude0
ClinVar
Risk rs796053107(;)
Alt rs796053107(;)
Reference rs796053107(ACCTCTAAGAG;ACCTCTAAGAG)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166866255_166866265delCTCTTAGAGGT
CLNSRC
CLNACC RCV000189099.1,