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rs267607021

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607021(A;A)
Make rs267607021(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position34425219
GeneFAM134C, RPS10
is asnp
is mentioned by
dbSNPrs267607021
ebirs267607021
HLIrs267607021
Exacrs267607021
Varsomers267607021
Maprs267607021
PheGenIrs267607021
hapmaprs267607021
1000 genomesrs267607021
hgdprs267607021
ensemblrs267607021
gopubmedrs267607021
geneviewrs267607021
scholarrs267607021
googlers267607021
pharmgkbrs267607021
gwascentralrs267607021
openSNPrs267607021
23andMers267607021
23andMe allrs267607021
SNP Nexus

SNPshotrs267607021
SNPdbers267607021
MSV3drs267607021
GWAS Ctlgrs267607021
Max Magnitude0
ClinVar
Risk rs267607021(A;A)
Alt rs267607021(A;A)
Reference rs267607021(G;G)
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.34392996C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006562.2,