rs121909624

Orientation

plus

Stabilized

plus

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

Make rs121909624(A;A)

Make rs121909624(A;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154567707

Gene

FGB

is a	snp
is	mentioned by
dbSNP	rs121909624
dbSNP (classic)	rs121909624
ClinGen	rs121909624
ebi	rs121909624
HLI	rs121909624
Exac	rs121909624
Gnomad	rs121909624
Varsome	rs121909624
LitVar	rs121909624
Map	rs121909624
PheGenI	rs121909624
Biobank	rs121909624
1000 genomes	rs121909624
hgdp	rs121909624
ensembl	rs121909624
geneview	rs121909624
scholar	rs121909624
google	rs121909624
pharmgkb	rs121909624
gwascentral	rs121909624
openSNP	rs121909624
23andMe	rs121909624
SNPshot	rs121909624
SNPdbe	rs121909624
MSV3d	rs121909624
GWAS Ctlg	rs121909624

Max Magnitude

0

OMIM	134830
Desc
Variant	0015
Related	also

ClinVar
Risk	rs121909624(A;A)
Alt	rs121909624(A;A)
Reference	Rs121909624(T;T)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	FGB
CLNDBN	Afibrinogenemia, congenital
Reversed	0
HGVS	NC_000004.11:g.155488859T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017821.25,