rs121909622

Orientation

plus

Stabilized

plus

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

Make rs121909622(A;A)

Make rs121909622(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154570463

Gene

FGB

is a	snp
is	mentioned by
dbSNP	rs121909622
dbSNP (classic)	rs121909622
ClinGen	rs121909622
ebi	rs121909622
HLI	rs121909622
Exac	rs121909622
Gnomad	rs121909622
Varsome	rs121909622
LitVar	rs121909622
Map	rs121909622
PheGenI	rs121909622
Biobank	rs121909622
1000 genomes	rs121909622
hgdp	rs121909622
ensembl	rs121909622
geneview	rs121909622
scholar	rs121909622
google	rs121909622
pharmgkb	rs121909622
gwascentral	rs121909622
openSNP	rs121909622
23andMe	rs121909622
SNPshot	rs121909622
SNPdbe	rs121909622
MSV3d	rs121909622
GWAS Ctlg	rs121909622

Max Magnitude

0

OMIM	134830
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121909622(A;A)
Alt	rs121909622(A;A)
Reference	Rs121909622(G;G)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	FGB
CLNDBN	Afibrinogenemia, congenital
Reversed	0
HGVS	NC_000004.11:g.155491615G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017816.28,