rs121913092

Orientation

minus

Stabilized

minus

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

Make rs121913092(A;G)

Make rs121913092(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154606770

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs121913092
dbSNP (classic)	rs121913092
ClinGen	rs121913092
ebi	rs121913092
HLI	rs121913092
Exac	rs121913092
Gnomad	rs121913092
Varsome	rs121913092
LitVar	rs121913092
Map	rs121913092
PheGenI	rs121913092
Biobank	rs121913092
1000 genomes	rs121913092
hgdp	rs121913092
ensembl	rs121913092
geneview	rs121913092
scholar	rs121913092
google	rs121913092
pharmgkb	rs121913092
gwascentral	rs121913092
openSNP	rs121913092
23andMe	rs121913092
SNPshot	rs121913092
SNPdbe	rs121913092
MSV3d	rs121913092
GWAS Ctlg	rs121913092

Max Magnitude

0

OMIM	134850
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121913092(G;G)
Alt	rs121913092(G;G)
Reference	Rs121913092(A;A)
Significance	Other
Disease	FIBRINOGEN NAGOYA 1
Variation	info
Gene	FGG
CLNDBN	FIBRINOGEN NAGOYA 1
Reversed	1
HGVS	NC_000004.11:g.155527922T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017788.1,