rs121913087

Orientation

minus

Stabilized

minus

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

Make rs121913087(C;T)

Make rs121913087(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154606933

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs121913087
dbSNP (classic)	rs121913087
ClinGen	rs121913087
ebi	rs121913087
HLI	rs121913087
Exac	rs121913087
Gnomad	rs121913087
Varsome	rs121913087
LitVar	rs121913087
Map	rs121913087
PheGenI	rs121913087
Biobank	rs121913087
1000 genomes	rs121913087
hgdp	rs121913087
ensembl	rs121913087
geneview	rs121913087
scholar	rs121913087
google	rs121913087
pharmgkb	rs121913087
gwascentral	rs121913087
openSNP	rs121913087
23andMe	rs121913087
SNPshot	rs121913087
SNPdbe	rs121913087
MSV3d	rs121913087
GWAS Ctlg	rs121913087

Max Magnitude

0

OMIM	134850
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121913087(T;T)
Alt	rs121913087(T;T)
Reference	Rs121913087(C;C)
Significance	Other
Disease	FIBRINOGEN TOKYO 2
Variation	info
Gene	FGG
CLNDBN	FIBRINOGEN TOKYO 2
Reversed	1
HGVS	NC_000004.11:g.155528085G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017772.5,