rs121913094

Orientation

minus

Stabilized

minus

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

Make rs121913094(A;T)

Make rs121913094(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154606767

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs121913094
dbSNP (classic)	rs121913094
ClinGen	rs121913094
ebi	rs121913094
HLI	rs121913094
Exac	rs121913094
Gnomad	rs121913094
Varsome	rs121913094
LitVar	rs121913094
Map	rs121913094
PheGenI	rs121913094
Biobank	rs121913094
1000 genomes	rs121913094
hgdp	rs121913094
ensembl	rs121913094
geneview	rs121913094
scholar	rs121913094
google	rs121913094
pharmgkb	rs121913094
gwascentral	rs121913094
openSNP	rs121913094
23andMe	rs121913094
SNPshot	rs121913094
SNPdbe	rs121913094
MSV3d	rs121913094
GWAS Ctlg	rs121913094

Max Magnitude

0

OMIM	134850
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121913094(T;T)
Alt	rs121913094(T;T)
Reference	Rs121913094(A;A)
Significance	Other
Disease	FIBRINOGEN MILANO 1
Variation	info
Gene	FGG
CLNDBN	FIBRINOGEN MILANO 1
Reversed	1
HGVS	NC_000004.11:g.155527919T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017790.5,