rs73015965

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs73015965(A;G)

Make rs73015965(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

160706469

Gene

PLG

is a	snp
is	mentioned by
dbSNP	rs73015965
dbSNP (classic)	rs73015965
ClinGen	rs73015965
ebi	rs73015965
HLI	rs73015965
Exac	rs73015965
Gnomad	rs73015965
Varsome	rs73015965
LitVar	rs73015965
Map	rs73015965
PheGenI	rs73015965
Biobank	rs73015965
1000 genomes	rs73015965
hgdp	rs73015965
ensembl	rs73015965
geneview	rs73015965
scholar	rs73015965
google	rs73015965
pharmgkb	rs73015965
gwascentral	rs73015965
openSNP	rs73015965
23andMe	rs73015965
SNPshot	rs73015965
SNPdbe	rs73015965
MSV3d	rs73015965
GWAS Ctlg	rs73015965

GMAF

0.002755

Max Magnitude

0

OMIM	173350
Desc
Variant	0010
Related	also

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 UniProtKB (protein)
CLNACC	RCV000014551.27,