rs267606784

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs267606784(C;G)

Make rs267606784(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

131858735

Gene

ENPP1

is a	snp
is	mentioned by
dbSNP	rs267606784
dbSNP (classic)	rs267606784
ClinGen	rs267606784
ebi	rs267606784
HLI	rs267606784
Exac	rs267606784
Gnomad	rs267606784
Varsome	rs267606784
LitVar	rs267606784
Map	rs267606784
PheGenI	rs267606784
Biobank	rs267606784
1000 genomes	rs267606784
hgdp	rs267606784
ensembl	rs267606784
geneview	rs267606784
scholar	rs267606784
google	rs267606784
pharmgkb	rs267606784
gwascentral	rs267606784
openSNP	rs267606784
23andMe	rs267606784
SNPshot	rs267606784
SNPdbe	rs267606784
MSV3d	rs267606784
GWAS Ctlg	rs267606784

Max Magnitude

0

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,