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rs121918029

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918029(C;C)
Make rs121918029(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position160736976
GenePLG
is asnp
is mentioned by
dbSNPrs121918029
ebirs121918029
HLIrs121918029
Exacrs121918029
Varsomers121918029
Maprs121918029
PheGenIrs121918029
hapmaprs121918029
1000 genomesrs121918029
hgdprs121918029
ensemblrs121918029
gopubmedrs121918029
geneviewrs121918029
scholarrs121918029
googlers121918029
pharmgkbrs121918029
gwascentralrs121918029
openSNPrs121918029
23andMers121918029
23andMe allrs121918029
SNP Nexus

SNPshotrs121918029
SNPdbers121918029
MSV3drs121918029
GWAS Ctlgrs121918029
Max Magnitude0
OMIM173350
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918029(C;C)
Alt rs121918029(C;C)
Reference rs121918029(T;T)
Significance Pathogenic
Disease Dysplasminogenemia
Variation info
Gene PLG
CLNDBN Dysplasminogenemia
Reversed 0
HGVS NC_000006.11:g.161158008T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014544.24,