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rs121918033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918033(A;A)
Make rs121918033(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position160752240
GenePLG
is asnp
is mentioned by
dbSNPrs121918033
ebirs121918033
HLIrs121918033
Exacrs121918033
Varsomers121918033
Maprs121918033
PheGenIrs121918033
hapmaprs121918033
1000 genomesrs121918033
hgdprs121918033
ensemblrs121918033
gopubmedrs121918033
geneviewrs121918033
scholarrs121918033
googlers121918033
pharmgkbrs121918033
gwascentralrs121918033
openSNPrs121918033
23andMers121918033
23andMe allrs121918033
SNP Nexus

SNPshotrs121918033
SNPdbers121918033
MSV3drs121918033
GWAS Ctlgrs121918033
Max Magnitude0
OMIM173350
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121918033(A;A)
Alt rs121918033(A;A)
Reference rs121918033(G;G)
Significance Pathogenic
Disease Dysplasminogenemia
Variation info
Gene PLG
CLNDBN Dysplasminogenemia
Reversed 0
HGVS NC_000006.11:g.161173272G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014548.24,