rs121913091

Orientation

minus

Stabilized

minus

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

Make rs121913091(C;C)

Make rs121913091(C;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154606827

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs121913091
dbSNP (classic)	rs121913091
ClinGen	rs121913091
ebi	rs121913091
HLI	rs121913091
Exac	rs121913091
Gnomad	rs121913091
Varsome	rs121913091
LitVar	rs121913091
Map	rs121913091
PheGenI	rs121913091
Biobank	rs121913091
1000 genomes	rs121913091
hgdp	rs121913091
ensembl	rs121913091
geneview	rs121913091
scholar	rs121913091
google	rs121913091
pharmgkb	rs121913091
gwascentral	rs121913091
openSNP	rs121913091
23andMe	rs121913091
SNPshot	rs121913091
SNPdbe	rs121913091
MSV3d	rs121913091
GWAS Ctlg	rs121913091

Max Magnitude

0

OMIM	134850
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121913091(C;C)
Alt	rs121913091(C;C)
Reference	Rs121913091(T;T)
Significance	Other
Disease	FIBRINOGEN ASAHI
Variation	info
Gene	FGG
CLNDBN	FIBRINOGEN ASAHI
Reversed	1
HGVS	NC_000004.11:g.155527979A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017786.2,