rs121909616

Orientation

plus

Stabilized

plus

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

Make rs121909616(C;T)

Make rs121909616(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154565823

Gene

FGB

is a	snp
is	mentioned by
dbSNP	rs121909616
dbSNP (classic)	rs121909616
ClinGen	rs121909616
ebi	rs121909616
HLI	rs121909616
Exac	rs121909616
Gnomad	rs121909616
Varsome	rs121909616
LitVar	rs121909616
Map	rs121909616
PheGenI	rs121909616
Biobank	rs121909616
1000 genomes	rs121909616
hgdp	rs121909616
ensembl	rs121909616
geneview	rs121909616
scholar	rs121909616
google	rs121909616
pharmgkb	rs121909616
gwascentral	rs121909616
openSNP	rs121909616
23andMe	rs121909616
SNPshot	rs121909616
SNPdbe	rs121909616
MSV3d	rs121909616
GWAS Ctlg	rs121909616

Max Magnitude

0

OMIM	134830
Desc
Variant	0002
Related	also

OMIM	134830
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121909616(T;T)
Alt	rs121909616(T;T)
Reference	Rs121909616(C;C)
Significance	Other
Disease	FIBRINOGEN CHRISTCHURCH 2
Variation	info
Gene	FGB
CLNDBN	FIBRINOGEN CHRISTCHURCH 2
Reversed	0
HGVS	NC_000004.11:g.155486975C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017804.5,