rs606231224

Orientation

plus

Stabilized

plus

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

Make rs606231224(G;T)

Make rs606231224(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

154569800

Gene

FGB

is a	snp
is	mentioned by
dbSNP	rs606231224
dbSNP (classic)	rs606231224
ClinGen	rs606231224
ebi	rs606231224
HLI	rs606231224
Exac	rs606231224
Gnomad	rs606231224
Varsome	rs606231224
LitVar	rs606231224
Map	rs606231224
PheGenI	rs606231224
Biobank	rs606231224
1000 genomes	rs606231224
hgdp	rs606231224
ensembl	rs606231224
geneview	rs606231224
scholar	rs606231224
google	rs606231224
pharmgkb	rs606231224
gwascentral	rs606231224
openSNP	rs606231224
23andMe	rs606231224
SNPshot	rs606231224
SNPdbe	rs606231224
MSV3d	rs606231224
GWAS Ctlg	rs606231224

Max Magnitude

0

ClinVar
Risk	rs606231224(T;T)
Alt	rs606231224(T;T)
Reference	Rs606231224(G;G)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	FGB
CLNDBN	Afibrinogenemia, congenital
Reversed	0
HGVS	NC_000004.11:g.155490952G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017819.27,