rs121918032

Orientation

plus

Stabilized

plus

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

Make rs121918032(G;T)

Make rs121918032(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

160731229

Gene

PLG

is a	snp
is	mentioned by
dbSNP	rs121918032
dbSNP (classic)	rs121918032
ClinGen	rs121918032
ebi	rs121918032
HLI	rs121918032
Exac	rs121918032
Gnomad	rs121918032
Varsome	rs121918032
LitVar	rs121918032
Map	rs121918032
PheGenI	rs121918032
Biobank	rs121918032
1000 genomes	rs121918032
hgdp	rs121918032
ensembl	rs121918032
geneview	rs121918032
scholar	rs121918032
google	rs121918032
pharmgkb	rs121918032
gwascentral	rs121918032
openSNP	rs121918032
23andMe	rs121918032
SNPshot	rs121918032
SNPdbe	rs121918032
MSV3d	rs121918032
GWAS Ctlg	rs121918032

Max Magnitude

0

OMIM	173350
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121918032(T;T)
Alt	rs121918032(T;T)
Reference	Rs121918032(G;G)
Significance	Pathogenic
Disease	Plasminogen deficiency
Variation	info
Gene	PLG
CLNDBN	Plasminogen deficiency, type I
Reversed	0
HGVS	NC_000006.11:g.161152261G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014547.19,