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rs606231210

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231210(-;-)
Make rs606231210(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position160741418
GenePLG
is asnp
is mentioned by
dbSNPrs606231210
ebirs606231210
HLIrs606231210
Exacrs606231210
Varsomers606231210
Maprs606231210
PheGenIrs606231210
hapmaprs606231210
1000 genomesrs606231210
hgdprs606231210
ensemblrs606231210
gopubmedrs606231210
geneviewrs606231210
scholarrs606231210
googlers606231210
pharmgkbrs606231210
gwascentralrs606231210
openSNPrs606231210
23andMers606231210
23andMe allrs606231210
SNP Nexus

SNPshotrs606231210
SNPdbers606231210
MSV3drs606231210
GWAS Ctlgrs606231210
Max Magnitude0
ClinVar
Risk rs606231210(;)
Alt rs606231210(;)
Reference rs606231210(G;G)
Significance Pathogenic
Disease Plasminogen deficiency
Variation info
Gene PLG
CLNDBN Plasminogen deficiency, type I
Reversed 0
HGVS NC_000006.11:g.161162450delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000014550.26,