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rs111320759

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111320759(C;T)
Make rs111320759(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position14884212
GeneMGP
is asnp
is mentioned by
dbSNPrs111320759
ebirs111320759
HLIrs111320759
Exacrs111320759
Varsomers111320759
Maprs111320759
PheGenIrs111320759
hapmaprs111320759
1000 genomesrs111320759
hgdprs111320759
ensemblrs111320759
gopubmedrs111320759
geneviewrs111320759
scholarrs111320759
googlers111320759
pharmgkbrs111320759
gwascentralrs111320759
openSNPrs111320759
23andMers111320759
23andMe allrs111320759
SNP Nexus

SNPshotrs111320759
SNPdbers111320759
MSV3drs111320759
GWAS Ctlgrs111320759
Max Magnitude0
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,