rs121918029

Orientation

plus

Stabilized

plus

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

Make rs121918029(C;C)

Make rs121918029(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

160736976

Gene

PLG

is a	snp
is	mentioned by
dbSNP	rs121918029
dbSNP (classic)	rs121918029
ClinGen	rs121918029
ebi	rs121918029
HLI	rs121918029
Exac	rs121918029
Gnomad	rs121918029
Varsome	rs121918029
LitVar	rs121918029
Map	rs121918029
PheGenI	rs121918029
Biobank	rs121918029
1000 genomes	rs121918029
hgdp	rs121918029
ensembl	rs121918029
geneview	rs121918029
scholar	rs121918029
google	rs121918029
pharmgkb	rs121918029
gwascentral	rs121918029
openSNP	rs121918029
23andMe	rs121918029
SNPshot	rs121918029
SNPdbe	rs121918029
MSV3d	rs121918029
GWAS Ctlg	rs121918029

Max Magnitude

0

OMIM	173350
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121918029(C;C)
Alt	rs121918029(C;C)
Reference	Rs121918029(T;T)
Significance	Pathogenic
Disease	Dysplasminogenemia
Variation	info
Gene	PLG
CLNDBN	Dysplasminogenemia
Reversed	0
HGVS	NC_000006.11:g.161158008T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014544.24,