rs121909625

Orientation

plus

Stabilized

plus

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

Make rs121909625(C;T)

Make rs121909625(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154565832

Gene

FGB

is a	snp
is	mentioned by
dbSNP	rs121909625
dbSNP (classic)	rs121909625
ClinGen	rs121909625
ebi	rs121909625
HLI	rs121909625
Exac	rs121909625
Gnomad	rs121909625
Varsome	rs121909625
LitVar	rs121909625
Map	rs121909625
PheGenI	rs121909625
Biobank	rs121909625
1000 genomes	rs121909625
hgdp	rs121909625
ensembl	rs121909625
geneview	rs121909625
scholar	rs121909625
google	rs121909625
pharmgkb	rs121909625
gwascentral	rs121909625
openSNP	rs121909625
23andMe	rs121909625
SNPshot	rs121909625
SNPdbe	rs121909625
MSV3d	rs121909625
GWAS Ctlg	rs121909625

Max Magnitude

0

OMIM	134830
Desc
Variant	0016
Related	also

ClinVar
Risk	rs121909625(T;T)
Alt	rs121909625(T;T)
Reference	Rs121909625(C;C)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	FGB
CLNDBN	Afibrinogenemia, congenital
Reversed	0
HGVS	NC_000004.11:g.155486984C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017822.30,