rs121913089

Orientation

minus

Stabilized

minus

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

Make rs121913089(G;T)

Make rs121913089(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154606881

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs121913089
dbSNP (classic)	rs121913089
ClinGen	rs121913089
ebi	rs121913089
HLI	rs121913089
Exac	rs121913089
Gnomad	rs121913089
Varsome	rs121913089
LitVar	rs121913089
Map	rs121913089
PheGenI	rs121913089
Biobank	rs121913089
1000 genomes	rs121913089
hgdp	rs121913089
ensembl	rs121913089
geneview	rs121913089
scholar	rs121913089
google	rs121913089
pharmgkb	rs121913089
gwascentral	rs121913089
openSNP	rs121913089
23andMe	rs121913089
SNPshot	rs121913089
SNPdbe	rs121913089
MSV3d	rs121913089
GWAS Ctlg	rs121913089

Max Magnitude

0

OMIM	134850
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121913089(T;T)
Alt	rs121913089(T;T)
Reference	Rs121913089(G;G)
Significance	Other
Disease	FIBRINOGEN BALTIMORE 1
Variation	info
Gene	FGG
CLNDBN	FIBRINOGEN BALTIMORE 1
Reversed	1
HGVS	NC_000004.11:g.155528033C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017783.3,