rs121909620

Orientation

plus

Stabilized

plus

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

Make rs121909620(A;A)

Make rs121909620(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154565985

Gene

FGB

is a	snp
is	mentioned by
dbSNP	rs121909620
dbSNP (classic)	rs121909620
ClinGen	rs121909620
ebi	rs121909620
HLI	rs121909620
Exac	rs121909620
Gnomad	rs121909620
Varsome	rs121909620
LitVar	rs121909620
Map	rs121909620
PheGenI	rs121909620
Biobank	rs121909620
1000 genomes	rs121909620
hgdp	rs121909620
ensembl	rs121909620
geneview	rs121909620
scholar	rs121909620
google	rs121909620
pharmgkb	rs121909620
gwascentral	rs121909620
openSNP	rs121909620
23andMe	rs121909620
SNPshot	rs121909620
SNPdbe	rs121909620
MSV3d	rs121909620
GWAS Ctlg	rs121909620

Max Magnitude

0

OMIM	134830
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121909620(A;A)
Alt	rs121909620(A;A)
Reference	Rs121909620(G;G)
Significance	Other
Disease	FIBRINOGEN NAPLES
Variation	info
Gene	FGB
CLNDBN	FIBRINOGEN NAPLES
Reversed	0
HGVS	NC_000004.11:g.155487137G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017811.5,