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rs770282904

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs770282904(C;C)
Make rs770282904(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position34938907
GeneDNAJC21
is asnp
is mentioned by
dbSNPrs770282904
ebirs770282904
HLIrs770282904
Exacrs770282904
Varsomers770282904
Maprs770282904
PheGenIrs770282904
hapmaprs770282904
1000 genomesrs770282904
hgdprs770282904
ensemblrs770282904
gopubmedrs770282904
geneviewrs770282904
scholarrs770282904
googlers770282904
pharmgkbrs770282904
gwascentralrs770282904
openSNPrs770282904
23andMers770282904
23andMe allrs770282904
SNP Nexus

SNPshotrs770282904
SNPdbers770282904
MSV3drs770282904
GWAS Ctlgrs770282904
Max Magnitude0
ClinVar
Risk rs770282904(C,T;C,T)
Alt rs770282904(C,T;C,T)
Reference rs770282904(G;G)
Significance Pathogenic
Disease Inherited bone marrow failure syndrome Bone marrow failure syndrome 3
Variation info
Gene DNAJC21
CLNDBN Inherited bone marrow failure syndrome Bone marrow failure syndrome 3
Reversed 0
HGVS NC_000005.9:g.34939012G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000237092.1, RCV000239519.1,