rs121909613

Orientation

minus

Stabilized

minus

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

Make rs121909613(C;T)

Make rs121909613(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154585712

Gene

FGA

is a	snp
is	mentioned by
dbSNP	rs121909613
dbSNP (classic)	rs121909613
ClinGen	rs121909613
ebi	rs121909613
HLI	rs121909613
Exac	rs121909613
Gnomad	rs121909613
Varsome	rs121909613
LitVar	rs121909613
Map	rs121909613
PheGenI	rs121909613
Biobank	rs121909613
1000 genomes	rs121909613
hgdp	rs121909613
ensembl	rs121909613
geneview	rs121909613
scholar	rs121909613
google	rs121909613
pharmgkb	rs121909613
gwascentral	rs121909613
openSNP	rs121909613
23andMe	rs121909613
SNPshot	rs121909613
SNPdbe	rs121909613
MSV3d	rs121909613
GWAS Ctlg	rs121909613

Max Magnitude

0

OMIM	134820
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121909613(A;A) rs121909613(G;G) rs121909613(T;T)
Alt	rs121909613(A;A) rs121909613(G;G) rs121909613(T;T)
Reference	Rs121909613(C;C)
Significance	Other
Disease	FIBRINOGEN DUSART
Variation	info
Gene	FGA
CLNDBN	FIBRINOGEN DUSART
Reversed	1
HGVS	NC_000004.11:g.155506864G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017872.6,