rs121909621

Orientation

plus

Stabilized

plus

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

Make rs121909621(G;G)

Make rs121909621(G;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154569703

Gene

FGB

is a	snp
is	mentioned by
dbSNP	rs121909621
dbSNP (classic)	rs121909621
ClinGen	rs121909621
ebi	rs121909621
HLI	rs121909621
Exac	rs121909621
Gnomad	rs121909621
Varsome	rs121909621
LitVar	rs121909621
Map	rs121909621
PheGenI	rs121909621
Biobank	rs121909621
1000 genomes	rs121909621
hgdp	rs121909621
ensembl	rs121909621
geneview	rs121909621
scholar	rs121909621
google	rs121909621
pharmgkb	rs121909621
gwascentral	rs121909621
openSNP	rs121909621
23andMe	rs121909621
SNPshot	rs121909621
SNPdbe	rs121909621
MSV3d	rs121909621
GWAS Ctlg	rs121909621

Max Magnitude

0

OMIM	134830
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121909621(G;G)
Alt	rs121909621(G;G)
Reference	Rs121909621(T;T)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	FGB
CLNDBN	Afibrinogenemia, congenital
Reversed	0
HGVS	NC_000004.11:g.155490855T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017815.28,