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rs267607022

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607022(C;T)
Make rs267607022(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position34421793
GeneFAM134C, RPS10
is asnp
is mentioned by
dbSNPrs267607022
ebirs267607022
HLIrs267607022
Exacrs267607022
Varsomers267607022
Maprs267607022
PheGenIrs267607022
hapmaprs267607022
1000 genomesrs267607022
hgdprs267607022
ensemblrs267607022
gopubmedrs267607022
geneviewrs267607022
scholarrs267607022
googlers267607022
pharmgkbrs267607022
gwascentralrs267607022
openSNPrs267607022
23andMers267607022
23andMe allrs267607022
SNP Nexus

SNPshotrs267607022
SNPdbers267607022
MSV3drs267607022
GWAS Ctlgrs267607022
Max Magnitude0
ClinVar
Risk rs267607022(T;T)
Alt rs267607022(T;T)
Reference rs267607022(C;C)
Significance Pathogenic
Disease Diamond-Blackfan anemia 9
Variation info
Gene RPS10-NUDT3 RPS10
CLNDBN Diamond-Blackfan anemia 9
Reversed 1
HGVS NC_000006.11:g.34389570G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006564.2,