rs121913090

Orientation

minus

Stabilized

minus

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

Make rs121913090(A;T)

Make rs121913090(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154606833

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs121913090
dbSNP (classic)	rs121913090
ClinGen	rs121913090
ebi	rs121913090
HLI	rs121913090
Exac	rs121913090
Gnomad	rs121913090
Varsome	rs121913090
LitVar	rs121913090
Map	rs121913090
PheGenI	rs121913090
Biobank	rs121913090
1000 genomes	rs121913090
hgdp	rs121913090
ensembl	rs121913090
geneview	rs121913090
scholar	rs121913090
google	rs121913090
pharmgkb	rs121913090
gwascentral	rs121913090
openSNP	rs121913090
23andMe	rs121913090
SNPshot	rs121913090
SNPdbe	rs121913090
MSV3d	rs121913090
GWAS Ctlg	rs121913090

GMAF

0.0004591

Max Magnitude

0

OMIM	134850
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121913090(T;T)
Alt	rs121913090(T;T)
Reference	Rs121913090(A;A)
Significance	Other
Disease	FIBRINOGEN BALTIMORE 3
Variation	info
Gene	FGG
CLNDBN	FIBRINOGEN BALTIMORE 3
Reversed	1
HGVS	NC_000004.11:g.155527985T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017785.2,