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rs587776907

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs587776907(-;-)
Make rs587776907(-;CA)
ReferenceGRCh38 38.1/142
Chromosome4
Position56484842
GeneSRP72
is asnp
is mentioned by
dbSNPrs587776907
ebirs587776907
HLIrs587776907
Exacrs587776907
Varsomers587776907
Maprs587776907
PheGenIrs587776907
hapmaprs587776907
1000 genomesrs587776907
hgdprs587776907
ensemblrs587776907
gopubmedrs587776907
geneviewrs587776907
scholarrs587776907
googlers587776907
pharmgkbrs587776907
gwascentralrs587776907
openSNPrs587776907
23andMers587776907
23andMe allrs587776907
SNP Nexus

SNPshotrs587776907
SNPdbers587776907
MSV3drs587776907
GWAS Ctlgrs587776907
Max Magnitude0
ClinVar
Risk rs587776907(;)
Alt rs587776907(;)
Reference rs587776907(CA;CA)
Significance Pathogenic
Disease Bone marrow failure syndrome 1
Variation info
Gene SRP72
CLNDBN Bone marrow failure syndrome 1
Reversed 0
HGVS NC_000004.11:g.57351008_57351009delCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000024352.4,