rs121913093

Orientation

minus

Stabilized

minus

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

Make rs121913093(G;T)

Make rs121913093(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154606768

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs121913093
dbSNP (classic)	rs121913093
ClinGen	rs121913093
ebi	rs121913093
HLI	rs121913093
Exac	rs121913093
Gnomad	rs121913093
Varsome	rs121913093
LitVar	rs121913093
Map	rs121913093
PheGenI	rs121913093
Biobank	rs121913093
1000 genomes	rs121913093
hgdp	rs121913093
ensembl	rs121913093
geneview	rs121913093
scholar	rs121913093
google	rs121913093
pharmgkb	rs121913093
gwascentral	rs121913093
openSNP	rs121913093
23andMe	rs121913093
SNPshot	rs121913093
SNPdbe	rs121913093
MSV3d	rs121913093
GWAS Ctlg	rs121913093

Max Magnitude

0

OMIM	134850
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121913093(T;T)
Alt	rs121913093(T;T)
Reference	Rs121913093(G;G)
Significance	Other
Disease	FIBRINOGEN KYOTO 3
Variation	info
Gene	FGG
CLNDBN	FIBRINOGEN KYOTO 3
Reversed	1
HGVS	NC_000004.11:g.155527920C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017789.1,