rs121913088

Orientation

minus

Stabilized

minus

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

Make rs121913088(A;A)

Make rs121913088(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154606932

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs121913088
dbSNP (classic)	rs121913088
ClinGen	rs121913088
ebi	rs121913088
HLI	rs121913088
Exac	rs121913088
Gnomad	rs121913088
Varsome	rs121913088
LitVar	rs121913088
Map	rs121913088
PheGenI	rs121913088
Biobank	rs121913088
1000 genomes	rs121913088
hgdp	rs121913088
ensembl	rs121913088
geneview	rs121913088
scholar	rs121913088
google	rs121913088
pharmgkb	rs121913088
gwascentral	rs121913088
openSNP	rs121913088
23andMe	rs121913088
SNPshot	rs121913088
SNPdbe	rs121913088
MSV3d	rs121913088
GWAS Ctlg	rs121913088

Max Magnitude

0

OMIM	134850
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121913088(A;A)
Alt	rs121913088(A;A)
Reference	Rs121913088(G;G)
Significance	Other
Disease	FIBRINOGEN HAIFA 1
Variation	info
Gene	FGG
CLNDBN	FIBRINOGEN HAIFA 1
Reversed	1
HGVS	NC_000004.11:g.155528084C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017777.4,