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rs121918028

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918028(G;T)
Make rs121918028(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position160722431
GenePLG
is asnp
is mentioned by
dbSNPrs121918028
ebirs121918028
HLIrs121918028
Exacrs121918028
Varsomers121918028
Maprs121918028
PheGenIrs121918028
hapmaprs121918028
1000 genomesrs121918028
hgdprs121918028
ensemblrs121918028
gopubmedrs121918028
geneviewrs121918028
scholarrs121918028
googlers121918028
pharmgkbrs121918028
gwascentralrs121918028
openSNPrs121918028
23andMers121918028
23andMe allrs121918028
SNP Nexus

SNPshotrs121918028
SNPdbers121918028
MSV3drs121918028
GWAS Ctlgrs121918028
GMAF0.0009183
Max Magnitude0
OMIM173350
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121918028(T;T)
Alt rs121918028(T;T)
Reference rs121918028(G;G)
Significance Pathogenic
Disease Dysplasminogenemia
Variation info
Gene PLG
CLNDBN Dysplasminogenemia
Reversed 0
HGVS NC_000006.11:g.161143463G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014543.25,