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rs587776953

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776953(-;-)
Make rs587776953(-;C)
Make rs587776953(C;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position76036026
GeneC10orf11
is asnp
is mentioned by
dbSNPrs587776953
ebirs587776953
HLIrs587776953
Exacrs587776953
Varsomers587776953
Maprs587776953
PheGenIrs587776953
hapmaprs587776953
1000 genomesrs587776953
hgdprs587776953
ensemblrs587776953
gopubmedrs587776953
geneviewrs587776953
scholarrs587776953
googlers587776953
pharmgkbrs587776953
gwascentralrs587776953
openSNPrs587776953
23andMers587776953
23andMe allrs587776953
SNP Nexus

SNPshotrs587776953
SNPdbers587776953
MSV3drs587776953
GWAS Ctlgrs587776953
Max Magnitude0
ClinVar
Risk rs587776953(C;C)
Alt rs587776953(C;C)
Reference rs587776953(;)
Significance Pathogenic
Disease Albinism
Variation info
Gene C10orf11
CLNDBN Albinism, oculocutaneous, type VII
Reversed 0
HGVS NC_000010.10:g.77795784dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000034834.4,