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rs587776698

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCTATCA;CCTATCA) 0 common in clinvar
Make rs587776698(-;-)
Make rs587776698(-;CTATCAC)
Make rs587776698(CTATCAC;CTATCAC)
ReferenceGRCh38 38.1/142
Chromosome4
Position87663263
GeneDMP1
is asnp
is mentioned by
dbSNPrs587776698
ebirs587776698
HLIrs587776698
Exacrs587776698
Varsomers587776698
Maprs587776698
PheGenIrs587776698
hapmaprs587776698
1000 genomesrs587776698
hgdprs587776698
ensemblrs587776698
gopubmedrs587776698
geneviewrs587776698
scholarrs587776698
googlers587776698
pharmgkbrs587776698
gwascentralrs587776698
openSNPrs587776698
23andMers587776698
23andMe allrs587776698
SNP Nexus

SNPshotrs587776698
SNPdbers587776698
MSV3drs587776698
GWAS Ctlgrs587776698
Max Magnitude0
ClinVar
Risk rs587776698(;)
Alt rs587776698(;)
Reference rs587776698(CCTATCA;CCTATCA)
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.88584415_88584421delCTATCAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000009107.3,