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rs587777101

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777101(A;G)
Make rs587777101(G;G)
ReferenceGRCh38 38.1/142
Chromosome15
Position36657840
GeneC15orf41
is asnp
is mentioned by
dbSNPrs587777101
ebirs587777101
HLIrs587777101
Exacrs587777101
Varsomers587777101
Maprs587777101
PheGenIrs587777101
hapmaprs587777101
1000 genomesrs587777101
hgdprs587777101
ensemblrs587777101
gopubmedrs587777101
geneviewrs587777101
scholarrs587777101
googlers587777101
pharmgkbrs587777101
gwascentralrs587777101
openSNPrs587777101
23andMers587777101
23andMe allrs587777101
SNP Nexus

SNPshotrs587777101
SNPdbers587777101
MSV3drs587777101
GWAS Ctlgrs587777101
Max Magnitude0
ClinVar
Risk rs587777101(C;C) rs587777101(G;G)
Alt rs587777101(C;C) rs587777101(G;G)
Reference Rs587777101(A;A)
Significance Pathogenic
Disease ANEMIA
Variation info
Gene C15orf41
CLNDBN ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib
Reversed 0
HGVS NC_000015.9:g.36950041A>G
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000083302.4,