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

rs797045919

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045919(C;T)
Make rs797045919(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position56042476
GeneLOC105369780, RPS26
is asnp
is mentioned by
dbSNPrs797045919
ebirs797045919
HLIrs797045919
Exacrs797045919
Varsomers797045919
Maprs797045919
PheGenIrs797045919
hapmaprs797045919
1000 genomesrs797045919
hgdprs797045919
ensemblrs797045919
gopubmedrs797045919
geneviewrs797045919
scholarrs797045919
googlers797045919
pharmgkbrs797045919
gwascentralrs797045919
openSNPrs797045919
23andMers797045919
23andMe allrs797045919
SNP Nexus

SNPshotrs797045919
SNPdbers797045919
MSV3drs797045919
GWAS Ctlgrs797045919
Max Magnitude0
ClinVar
Risk rs797045919(T;T)
Alt rs797045919(T;T)
Reference rs797045919(C;C)
Significance Pathogenic
Disease Diamond-Blackfan anemia 10
Variation info
Gene RPS26
CLNDBN Diamond-Blackfan anemia 10
Reversed 0
HGVS NC_000012.11:g.56436260C>T
CLNSRC
CLNACC RCV000195166.1,