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rs121918032

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918032(G;T)
Make rs121918032(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position160731229
GenePLG
is asnp
is mentioned by
dbSNPrs121918032
ebirs121918032
HLIrs121918032
Exacrs121918032
Varsomers121918032
Maprs121918032
PheGenIrs121918032
hapmaprs121918032
1000 genomesrs121918032
hgdprs121918032
ensemblrs121918032
gopubmedrs121918032
geneviewrs121918032
scholarrs121918032
googlers121918032
pharmgkbrs121918032
gwascentralrs121918032
openSNPrs121918032
23andMers121918032
23andMe allrs121918032
SNP Nexus

SNPshotrs121918032
SNPdbers121918032
MSV3drs121918032
GWAS Ctlgrs121918032
Max Magnitude0
OMIM173350
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121918032(T;T)
Alt rs121918032(T;T)
Reference rs121918032(G;G)
Significance Pathogenic
Disease Plasminogen deficiency
Variation info
Gene PLG
CLNDBN Plasminogen deficiency, type I
Reversed 0
HGVS NC_000006.11:g.161152261G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014547.19,