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rs148622862

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148622862(A;A)
Make rs148622862(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position56042170
GeneLOC105369780, RPS26
is asnp
is mentioned by
dbSNPrs148622862
ebirs148622862
HLIrs148622862
Exacrs148622862
Varsomers148622862
Maprs148622862
PheGenIrs148622862
hapmaprs148622862
1000 genomesrs148622862
hgdprs148622862
ensemblrs148622862
gopubmedrs148622862
geneviewrs148622862
scholarrs148622862
googlers148622862
pharmgkbrs148622862
gwascentralrs148622862
openSNPrs148622862
23andMers148622862
23andMe allrs148622862
SNP Nexus

SNPshotrs148622862
SNPdbers148622862
MSV3drs148622862
GWAS Ctlgrs148622862
Max Magnitude0
ClinVar
Risk rs148622862(A;A)
Alt rs148622862(A;A)
Reference rs148622862(G;G)
Significance Pathogenic
Disease Diamond-Blackfan anemia 10
Variation info
Gene RPS26
CLNDBN Diamond-Blackfan anemia 10
Reversed 0
HGVS NC_000012.11:g.56435954G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006500.3,