rs121909615

Orientation

minus

Stabilized

minus

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

Make rs121909615(C;T)

Make rs121909615(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154586390

Gene

FGA

is a	snp
is	mentioned by
dbSNP	rs121909615
dbSNP (classic)	rs121909615
ClinGen	rs121909615
ebi	rs121909615
HLI	rs121909615
Exac	rs121909615
Gnomad	rs121909615
Varsome	rs121909615
LitVar	rs121909615
Map	rs121909615
PheGenI	rs121909615
Biobank	rs121909615
1000 genomes	rs121909615
hgdp	rs121909615
ensembl	rs121909615
geneview	rs121909615
scholar	rs121909615
google	rs121909615
pharmgkb	rs121909615
gwascentral	rs121909615
openSNP	rs121909615
23andMe	rs121909615
SNPshot	rs121909615
SNPdbe	rs121909615
MSV3d	rs121909615
GWAS Ctlg	rs121909615

Max Magnitude

0

OMIM	134820
Desc
Variant	0024
Related	also

ClinVar
Risk	rs121909615(T;T)
Alt	rs121909615(T;T)
Reference	Rs121909615(C;C)
Significance	Other
Disease	FIBRINOGEN KEOKUK
Variation	info
Gene	FGA
CLNDBN	FIBRINOGEN KEOKUK
Reversed	1
HGVS	NC_000004.11:g.155507542G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017880.3,