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rs61762293

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61762293(C;T)
Make rs61762293(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position41869138
GeneMIR6797, RPS19
is asnp
is mentioned by
dbSNPrs61762293
ebirs61762293
HLIrs61762293
Exacrs61762293
Varsomers61762293
Maprs61762293
PheGenIrs61762293
hapmaprs61762293
1000 genomesrs61762293
hgdprs61762293
ensemblrs61762293
gopubmedrs61762293
geneviewrs61762293
scholarrs61762293
googlers61762293
pharmgkbrs61762293
gwascentralrs61762293
openSNPrs61762293
23andMers61762293
23andMe allrs61762293
SNP Nexus

SNPshotrs61762293
SNPdbers61762293
MSV3drs61762293
GWAS Ctlgrs61762293
Max Magnitude0
OMIM603474
Desc
Variant0001
Relatedalso
ClinVar
Risk rs61762293(T;T)
Alt rs61762293(T;T)
Reference rs61762293(C;C)
Significance Pathogenic
Disease Diamond-Blackfan anemia 1
Variation info
Gene MIR6797 RPS19
CLNDBN Diamond-Blackfan anemia 1
Reversed 0
HGVS NC_000019.9:g.42373208C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033182.3,