Have questions? Visit https://www.reddit.com/r/SNPedia

rs148402804

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148402804(C;G)
Make rs148402804(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151289853
GeneZNF687
is asnp
is mentioned by
dbSNPrs148402804
ebirs148402804
HLIrs148402804
Exacrs148402804
Varsomers148402804
Maprs148402804
PheGenIrs148402804
hapmaprs148402804
1000 genomesrs148402804
hgdprs148402804
ensemblrs148402804
gopubmedrs148402804
geneviewrs148402804
scholarrs148402804
googlers148402804
pharmgkbrs148402804
gwascentralrs148402804
openSNPrs148402804
23andMers148402804
23andMe allrs148402804
SNP Nexus

SNPshotrs148402804
SNPdbers148402804
MSV3drs148402804
GWAS Ctlgrs148402804
Max Magnitude0
ClinVar
Risk rs148402804(A,G,T;A,G,T)
Alt rs148402804(A,G,T;A,G,T)
Reference rs148402804(C;C)
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.151262329C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000208586.1,