rs121909608

Orientation

minus

Stabilized

minus

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

Make rs121909608(A;G)

Make rs121909608(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154589505

Gene

FGA

is a	snp
is	mentioned by
dbSNP	rs121909608
dbSNP (classic)	rs121909608
ClinGen	rs121909608
ebi	rs121909608
HLI	rs121909608
Exac	rs121909608
Gnomad	rs121909608
Varsome	rs121909608
LitVar	rs121909608
Map	rs121909608
PheGenI	rs121909608
Biobank	rs121909608
1000 genomes	rs121909608
hgdp	rs121909608
ensembl	rs121909608
geneview	rs121909608
scholar	rs121909608
google	rs121909608
pharmgkb	rs121909608
gwascentral	rs121909608
openSNP	rs121909608
23andMe	rs121909608
SNPshot	rs121909608
SNPdbe	rs121909608
MSV3d	rs121909608
GWAS Ctlg	rs121909608

Max Magnitude

0

OMIM	134820
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121909608(G;G)
Alt	rs121909608(G;G)
Reference	Rs121909608(A;A)
Significance	Other
Disease	FIBRINOGEN AARHUS 1
Variation	info
Gene	FGA
CLNDBN	FIBRINOGEN AARHUS 1
Reversed	1
HGVS	NC_000004.11:g.155510657T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017843.1,