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rs587777100

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777100(A;A)
Make rs587777100(A;T)
ReferenceGRCh38 38.1/142
Chromosome15
Position36697379
GeneC15orf41
is asnp
is mentioned by
dbSNPrs587777100
ebirs587777100
HLIrs587777100
Exacrs587777100
Varsomers587777100
Maprs587777100
PheGenIrs587777100
hapmaprs587777100
1000 genomesrs587777100
hgdprs587777100
ensemblrs587777100
gopubmedrs587777100
geneviewrs587777100
scholarrs587777100
googlers587777100
pharmgkbrs587777100
gwascentralrs587777100
openSNPrs587777100
23andMers587777100
23andMe allrs587777100
SNP Nexus

SNPshotrs587777100
SNPdbers587777100
MSV3drs587777100
GWAS Ctlgrs587777100
Max Magnitude0
ClinVar
Risk rs587777100(A;A)
Alt rs587777100(A;A)
Reference rs587777100(T;T)
Significance Pathogenic
Disease ANEMIA
Variation info
Gene C15orf41
CLNDBN ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib
Reversed 0
HGVS NC_000015.9:g.36989580T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000083301.4,