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

rs121918025

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918025(G;T)
Make rs121918025(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position131861704
GeneENPP1
is asnp
is mentioned by
dbSNPrs121918025
ebirs121918025
HLIrs121918025
Exacrs121918025
Varsomers121918025
Maprs121918025
PheGenIrs121918025
hapmaprs121918025
1000 genomesrs121918025
hgdprs121918025
ensemblrs121918025
gopubmedrs121918025
geneviewrs121918025
scholarrs121918025
googlers121918025
pharmgkbrs121918025
gwascentralrs121918025
openSNPrs121918025
23andMers121918025
23andMe allrs121918025
SNP Nexus

SNPshotrs121918025
SNPdbers121918025
MSV3drs121918025
GWAS Ctlgrs121918025
Max Magnitude0
OMIM173335
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121918025(T;T)
Alt rs121918025(T;T)
Reference rs121918025(G;G)
Significance Pathogenic
Disease Arterial calcification of infancy
Variation info
Gene ENPP1
CLNDBN Arterial calcification of infancy
Reversed 0
HGVS NC_000006.11:g.132182844G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014560.25,