rs606231223

Orientation

plus

Stabilized

plus

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

Make rs606231223(C;T)

Make rs606231223(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

154569320

Gene

FGB

is a	snp
is	mentioned by
dbSNP	rs606231223
dbSNP (classic)	rs606231223
ClinGen	rs606231223
ebi	rs606231223
HLI	rs606231223
Exac	rs606231223
Gnomad	rs606231223
Varsome	rs606231223
LitVar	rs606231223
Map	rs606231223
PheGenI	rs606231223
Biobank	rs606231223
1000 genomes	rs606231223
hgdp	rs606231223
ensembl	rs606231223
geneview	rs606231223
scholar	rs606231223
google	rs606231223
pharmgkb	rs606231223
gwascentral	rs606231223
openSNP	rs606231223
23andMe	rs606231223
SNPshot	rs606231223
SNPdbe	rs606231223
MSV3d	rs606231223
GWAS Ctlg	rs606231223

Max Magnitude

0

ClinVar
Risk	rs606231223(T;T)
Alt	rs606231223(T;T)
Reference	Rs606231223(C;C)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	FGB
CLNDBN	Afibrinogenemia, congenital
Reversed	0
HGVS	NC_000004.11:g.155490472C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017818.27,