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

rs397518451

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs397518451(-;-)
Make rs397518451(-;GA)
ReferenceGRCh38 38.1/141
Chromosome17
Position8382190
GeneRPL26
is asnp
is mentioned by
dbSNPrs397518451
ebirs397518451
HLIrs397518451
Exacrs397518451
Varsomers397518451
Maprs397518451
PheGenIrs397518451
hapmaprs397518451
1000 genomesrs397518451
hgdprs397518451
ensemblrs397518451
gopubmedrs397518451
geneviewrs397518451
scholarrs397518451
googlers397518451
pharmgkbrs397518451
gwascentralrs397518451
openSNPrs397518451
23andMers397518451
23andMe allrs397518451
SNP Nexus

SNPshotrs397518451
SNPdbers397518451
MSV3drs397518451
GWAS Ctlgrs397518451
Max Magnitude0
ClinVar
Risk rs397518451(;)
Alt rs397518451(;)
Reference rs397518451(GA;GA)
Significance Pathogenic
Disease Diamond-Blackfan anemia 11
Variation info
Gene RPL26
CLNDBN Diamond-Blackfan anemia 11
Reversed 1
HGVS NC_000017.10:g.8285508_8285509delTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000032955.3,