rs121909611

Orientation

minus

Stabilized

minus

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

Make rs121909611(A;T)

Make rs121909611(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154585991

Gene

FGA

is a	snp
is	mentioned by
dbSNP	rs121909611
dbSNP (classic)	rs121909611
ClinGen	rs121909611
ebi	rs121909611
HLI	rs121909611
Exac	rs121909611
Gnomad	rs121909611
Varsome	rs121909611
LitVar	rs121909611
Map	rs121909611
PheGenI	rs121909611
Biobank	rs121909611
1000 genomes	rs121909611
hgdp	rs121909611
ensembl	rs121909611
geneview	rs121909611
scholar	rs121909611
google	rs121909611
pharmgkb	rs121909611
gwascentral	rs121909611
openSNP	rs121909611
23andMe	rs121909611
SNPshot	rs121909611
SNPdbe	rs121909611
MSV3d	rs121909611
GWAS Ctlg	rs121909611

Max Magnitude

0

OMIM	134820
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121909611(T;T)
Alt	rs121909611(T;T)
Reference	Rs121909611(A;A)
Significance	Other
Disease	FIBRINOGEN MARBURG
Variation	info
Gene	FGA
CLNDBN	FIBRINOGEN MARBURG
Reversed	1
HGVS	NC_000004.11:g.155507143T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017867.4,