rs121909617

Orientation

plus

Stabilized

plus

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

Make rs121909617(A;A)

Make rs121909617(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154569648

Gene

FGB

is a	snp
is	mentioned by
dbSNP	rs121909617
dbSNP (classic)	rs121909617
ClinGen	rs121909617
ebi	rs121909617
HLI	rs121909617
Exac	rs121909617
Gnomad	rs121909617
Varsome	rs121909617
LitVar	rs121909617
Map	rs121909617
PheGenI	rs121909617
Biobank	rs121909617
1000 genomes	rs121909617
hgdp	rs121909617
ensembl	rs121909617
geneview	rs121909617
scholar	rs121909617
google	rs121909617
pharmgkb	rs121909617
gwascentral	rs121909617
openSNP	rs121909617
23andMe	rs121909617
SNPshot	rs121909617
SNPdbe	rs121909617
MSV3d	rs121909617
GWAS Ctlg	rs121909617

Max Magnitude

0

OMIM	134830
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121909617(A;A)
Alt	rs121909617(A;A)
Reference	Rs121909617(G;G)
Significance	Other
Disease	FIBRINOGEN PONTOISE 2
Variation	info
Gene	FGB
CLNDBN	FIBRINOGEN PONTOISE 2
Reversed	0
HGVS	NC_000004.11:g.155490800G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017807.1,