Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515328

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515328(A;T)
Make rs397515328(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position119101571
GeneDPAGT1
is asnp
is mentioned by
dbSNPrs397515328
ebirs397515328
HLIrs397515328
Exacrs397515328
Varsomers397515328
Maprs397515328
PheGenIrs397515328
hapmaprs397515328
1000 genomesrs397515328
hgdprs397515328
ensemblrs397515328
gopubmedrs397515328
geneviewrs397515328
scholarrs397515328
googlers397515328
pharmgkbrs397515328
gwascentralrs397515328
openSNPrs397515328
23andMers397515328
23andMe allrs397515328
SNP Nexus

SNPshotrs397515328
SNPdbers397515328
MSV3drs397515328
GWAS Ctlgrs397515328
Max Magnitude0
ClinVar
Risk rs397515328(G,T;G,T)
Alt rs397515328(G,T;G,T)
Reference rs397515328(A;A)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 1J
Variation info
Gene DPAGT1
CLNDBN Congenital disorder of glycosylation type 1J
Reversed 1
HGVS NC_000011.9:g.118972281T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000055660.25,