Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052246

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052246(C;T)
Make rs796052246(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position40361333
GeneADSL
is asnp
is mentioned by
dbSNPrs796052246
ebirs796052246
HLIrs796052246
Exacrs796052246
Varsomers796052246
Maprs796052246
PheGenIrs796052246
hapmaprs796052246
1000 genomesrs796052246
hgdprs796052246
ensemblrs796052246
gopubmedrs796052246
geneviewrs796052246
scholarrs796052246
googlers796052246
pharmgkbrs796052246
gwascentralrs796052246
openSNPrs796052246
23andMers796052246
23andMe allrs796052246
SNP Nexus

SNPshotrs796052246
SNPdbers796052246
MSV3drs796052246
GWAS Ctlgrs796052246
Max Magnitude0
ClinVar
Risk rs796052246(T;T)
Alt rs796052246(T;T)
Reference rs796052246(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ADSL
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.40757337C>T
CLNSRC
CLNACC RCV000186679.1,