rs121909614

Orientation

minus

Stabilized

minus

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

Make rs121909614(A;A)

Make rs121909614(A;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154589501

Gene

FGA

is a	snp
is	mentioned by
dbSNP	rs121909614
dbSNP (classic)	rs121909614
ClinGen	rs121909614
ebi	rs121909614
HLI	rs121909614
Exac	rs121909614
Gnomad	rs121909614
Varsome	rs121909614
LitVar	rs121909614
Map	rs121909614
PheGenI	rs121909614
Biobank	rs121909614
1000 genomes	rs121909614
hgdp	rs121909614
ensembl	rs121909614
geneview	rs121909614
scholar	rs121909614
google	rs121909614
pharmgkb	rs121909614
gwascentral	rs121909614
openSNP	rs121909614
23andMe	rs121909614
SNPshot	rs121909614
SNPdbe	rs121909614
MSV3d	rs121909614
GWAS Ctlg	rs121909614

Max Magnitude

0

OMIM	134820
Desc
Variant	0015
Related	also

ClinVar
Risk	rs121909614(A;A)
Alt	rs121909614(A;A)
Reference	Rs121909614(T;T)
Significance	Other
Disease	FIBRINOGEN CANTERBURY
Variation	info
Gene	FGA
CLNDBN	FIBRINOGEN CANTERBURY
Reversed	1
HGVS	NC_000004.11:g.155510653A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017874.2,