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rs587776697

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776697(C;C)
Make rs587776697(C;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position87657031
GeneDMP1
is asnp
is mentioned by
dbSNPrs587776697
ebirs587776697
HLIrs587776697
Exacrs587776697
Varsomers587776697
Maprs587776697
PheGenIrs587776697
hapmaprs587776697
1000 genomesrs587776697
hgdprs587776697
ensemblrs587776697
gopubmedrs587776697
geneviewrs587776697
scholarrs587776697
googlers587776697
pharmgkbrs587776697
gwascentralrs587776697
openSNPrs587776697
23andMers587776697
23andMe allrs587776697
SNP Nexus

SNPshotrs587776697
SNPdbers587776697
MSV3drs587776697
GWAS Ctlgrs587776697
Max Magnitude0
ClinVar
Risk rs587776697(C;C)
Alt rs587776697(C;C)
Reference rs587776697(G;G)
Significance Pathogenic
Disease Autosomal recessive hypophosphatemic vitamin D refractory rickets
Variation info
Gene DMP1
CLNDBN Autosomal recessive hypophosphatemic vitamin D refractory rickets
Reversed 0
HGVS NC_000004.11:g.88578183G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009105.3,