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rs869025582

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025582(G;T)
Make rs869025582(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position151287016
GeneZNF687
is asnp
is mentioned by
dbSNPrs869025582
ebirs869025582
HLIrs869025582
Exacrs869025582
Varsomers869025582
Maprs869025582
PheGenIrs869025582
hapmaprs869025582
1000 genomesrs869025582
hgdprs869025582
ensemblrs869025582
gopubmedrs869025582
geneviewrs869025582
scholarrs869025582
googlers869025582
pharmgkbrs869025582
gwascentralrs869025582
openSNPrs869025582
23andMers869025582
23andMe allrs869025582
SNP Nexus

SNPshotrs869025582
SNPdbers869025582
MSV3drs869025582
GWAS Ctlgrs869025582
Max Magnitude0
ClinVar
Risk rs869025582(T;T)
Alt rs869025582(T;T)
Reference rs869025582(G;G)
Significance Pathogenic
Disease Paget disease of bone 6
Variation info
Gene ZNF687
CLNDBN Paget disease of bone 6
Reversed 0
HGVS NC_000001.10:g.151259492G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000208590.1,