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rs796053077

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053077(-;-)
Make rs796053077(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166002590
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053077
ebirs796053077
HLIrs796053077
Exacrs796053077
Varsomers796053077
Maprs796053077
PheGenIrs796053077
hapmaprs796053077
1000 genomesrs796053077
hgdprs796053077
ensemblrs796053077
gopubmedrs796053077
geneviewrs796053077
scholarrs796053077
googlers796053077
pharmgkbrs796053077
gwascentralrs796053077
openSNPrs796053077
23andMers796053077
23andMe allrs796053077
SNP Nexus

SNPshotrs796053077
SNPdbers796053077
MSV3drs796053077
GWAS Ctlgrs796053077
Max Magnitude0
ClinVar
Risk rs796053077(;)
Alt rs796053077(;)
Reference rs796053077(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166859100delT
CLNSRC
CLNACC RCV000189057.1,