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rs267607023

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Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607023(A;A)
Make rs267607023(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position56042518
GeneRPS26
is asnp
is mentioned by
dbSNPrs267607023
ebirs267607023
HLIrs267607023
Exacrs267607023
Varsomers267607023
Maprs267607023
PheGenIrs267607023
hapmaprs267607023
1000 genomesrs267607023
hgdprs267607023
ensemblrs267607023
gopubmedrs267607023
geneviewrs267607023
scholarrs267607023
googlers267607023
pharmgkbrs267607023
gwascentralrs267607023
openSNPrs267607023
23andMers267607023
23andMe allrs267607023
SNP Nexus

SNPshotrs267607023
SNPdbers267607023
MSV3drs267607023
GWAS Ctlgrs267607023
Max Magnitude0
ClinVar
Risk rs267607023(A;A)
Alt rs267607023(A;A)
Reference rs267607023(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.56436302G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006498.3,