rs121913095

Orientation

minus

Stabilized

minus

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

Make rs121913095(C;C)

Make rs121913095(C;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154605028

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs121913095
dbSNP (classic)	rs121913095
ClinGen	rs121913095
ebi	rs121913095
HLI	rs121913095
Exac	rs121913095
Gnomad	rs121913095
Varsome	rs121913095
LitVar	rs121913095
Map	rs121913095
PheGenI	rs121913095
Biobank	rs121913095
1000 genomes	rs121913095
hgdp	rs121913095
ensembl	rs121913095
geneview	rs121913095
scholar	rs121913095
google	rs121913095
pharmgkb	rs121913095
gwascentral	rs121913095
openSNP	rs121913095
23andMe	rs121913095
SNPshot	rs121913095
SNPdbe	rs121913095
MSV3d	rs121913095
GWAS Ctlg	rs121913095

Max Magnitude

0

OMIM	134850
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121913095(C;C)
Alt	rs121913095(C;C)
Reference	Rs121913095(G;G)
Significance	Other
Disease	FIBRINOGEN MATSUMOTO 1
Variation	info
Gene	FGG
CLNDBN	FIBRINOGEN MATSUMOTO 1
Reversed	1
HGVS	NC_000004.11:g.155526180C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017796.2,