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rs267606784

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606784(C;G)
Make rs267606784(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position131858735
GeneENPP1
is asnp
is mentioned by
dbSNPrs267606784
ebirs267606784
HLIrs267606784
Exacrs267606784
Varsomers267606784
Maprs267606784
PheGenIrs267606784
hapmaprs267606784
1000 genomesrs267606784
hgdprs267606784
ensemblrs267606784
gopubmedrs267606784
geneviewrs267606784
scholarrs267606784
googlers267606784
pharmgkbrs267606784
gwascentralrs267606784
openSNPrs267606784
23andMers267606784
23andMe allrs267606784
SNP Nexus

SNPshotrs267606784
SNPdbers267606784
MSV3drs267606784
GWAS Ctlgrs267606784
Max Magnitude0
ClinVar
Risk rs267606784(G;G)
Alt rs267606784(G;G)
Reference rs267606784(C;C)
Significance Pathogenic
Disease Arterial calcification of infancy
Variation info
Gene ENPP1
CLNDBN Arterial calcification of infancy
Reversed 0
HGVS NC_000006.11:g.132179875C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014567.20,