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rs73015965

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs73015965(A;G)
Make rs73015965(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position160706469
GenePLG
is asnp
is mentioned by
dbSNPrs73015965
ebirs73015965
HLIrs73015965
Exacrs73015965
Varsomers73015965
Maprs73015965
PheGenIrs73015965
hapmaprs73015965
1000 genomesrs73015965
hgdprs73015965
ensemblrs73015965
gopubmedrs73015965
geneviewrs73015965
scholarrs73015965
googlers73015965
pharmgkbrs73015965
gwascentralrs73015965
openSNPrs73015965
23andMers73015965
23andMe allrs73015965
SNP Nexus

SNPshotrs73015965
SNPdbers73015965
MSV3drs73015965
GWAS Ctlgrs73015965
GMAF0.002755
Max Magnitude0
OMIM173350
Desc
Variant0010
Relatedalso
ClinVar
Risk rs73015965(G;G)
Alt rs73015965(G;G)
Reference rs73015965(A;A)
Significance Pathogenic
Disease Plasminogen deficiency
Variation info
Gene PLG
CLNDBN Plasminogen deficiency, type I
Reversed 0
HGVS NC_000006.11:g.161127501A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014551.25,