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rs1057516424

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516424(A;T)
Make rs1057516424(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position74893302
GeneMPI
is asnp
is mentioned by
dbSNPrs1057516424
dbSNP (old)rs1057516424
ClinGenrs1057516424
ebirs1057516424
HLIrs1057516424
Exacrs1057516424
Gnomadrs1057516424
Varsomers1057516424
LitVarrs1057516424
Maprs1057516424
PheGenIrs1057516424
Biobankrs1057516424
1000 genomesrs1057516424
hgdprs1057516424
ensemblrs1057516424
gopubmedrs1057516424
geneviewrs1057516424
scholarrs1057516424
googlers1057516424
pharmgkbrs1057516424
gwascentralrs1057516424
openSNPrs1057516424
23andMers1057516424
23andMe allrs1057516424
SNPshotrs1057516424
SNPdbers1057516424
MSV3drs1057516424
GWAS Ctlgrs1057516424
Max Magnitude0
ClinVar
Risk rs1057516424(T;T)
Alt rs1057516424(T;T)
Reference Rs1057516424(A;A)
Significance Probable-Pathogenic
Disease Congenital disorder of glycosylation type 1B
Variation info
Gene MPI
CLNDBN Congenital disorder of glycosylation type 1B
Reversed 0
HGVS NC_000015.9:g.75185643A>T
CLNSRC
CLNACC RCV000410869.1,