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rs112518413

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs112518413(A;A)
Make rs112518413(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position14884247
GeneMGP
is asnp
is mentioned by
dbSNPrs112518413
ebirs112518413
HLIrs112518413
Exacrs112518413
Varsomers112518413
Maprs112518413
PheGenIrs112518413
hapmaprs112518413
1000 genomesrs112518413
hgdprs112518413
ensemblrs112518413
gopubmedrs112518413
geneviewrs112518413
scholarrs112518413
googlers112518413
pharmgkbrs112518413
gwascentralrs112518413
openSNPrs112518413
23andMers112518413
23andMe allrs112518413
SNP Nexus

SNPshotrs112518413
SNPdbers112518413
MSV3drs112518413
GWAS Ctlgrs112518413
Max Magnitude0
ClinVar
Risk rs112518413(A,C;A,C)
Alt rs112518413(A,C;A,C)
Reference rs112518413(T;T)
Significance Pathogenic
Disease Keutel syndrome
Variation info
Gene MGP
CLNDBN Keutel syndrome
Reversed 0
HGVS NC_000012.11:g.15037181T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015416.26,