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rs878854351

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854351(A;A)
Make rs878854351(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position76047256
GeneC10orf11
is asnp
is mentioned by
dbSNPrs878854351
ebirs878854351
HLIrs878854351
Exacrs878854351
Varsomers878854351
Maprs878854351
PheGenIrs878854351
hapmaprs878854351
1000 genomesrs878854351
hgdprs878854351
ensemblrs878854351
gopubmedrs878854351
geneviewrs878854351
scholarrs878854351
googlers878854351
pharmgkbrs878854351
gwascentralrs878854351
openSNPrs878854351
23andMers878854351
23andMe allrs878854351
SNP Nexus

SNPshotrs878854351
SNPdbers878854351
MSV3drs878854351
GWAS Ctlgrs878854351
Max Magnitude0
ClinVar
Risk rs878854351(A;A)
Alt rs878854351(A;A)
Reference rs878854351(C;C)
Significance Probable-Pathogenic
Disease Albinism
Variation info
Gene C10orf11
CLNDBN Albinism, oculocutaneous, type VII
Reversed 0
HGVS NC_000010.10:g.77807014C>A
CLNSRC
CLNACC RCV000234797.1,