rs111320759

Orientation

plus

Stabilized

plus

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

Make rs111320759(C;T)

Make rs111320759(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

14884212

Gene

MGP

is a	snp
is	mentioned by
dbSNP	rs111320759
dbSNP (classic)	rs111320759
ClinGen	rs111320759
ebi	rs111320759
HLI	rs111320759
Exac	rs111320759
Gnomad	rs111320759
Varsome	rs111320759
LitVar	rs111320759
Map	rs111320759
PheGenI	rs111320759
Biobank	rs111320759
1000 genomes	rs111320759
hgdp	rs111320759
ensembl	rs111320759
geneview	rs111320759
scholar	rs111320759
google	rs111320759
pharmgkb	rs111320759
gwascentral	rs111320759
openSNP	rs111320759
23andMe	rs111320759
SNPshot	rs111320759
SNPdbe	rs111320759
MSV3d	rs111320759
GWAS Ctlg	rs111320759

Max Magnitude

0

ClinVar
Risk	rs111320759(T;T)
Alt	rs111320759(T;T)
Reference	Rs111320759(C;C)
Significance	Pathogenic
Disease	Keutel syndrome
Variation	info
Gene	MGP
CLNDBN	Keutel syndrome
Reversed	0
HGVS	NC_000012.11:g.15037146C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015418.22,