rs587777720

Orientation

plus

Stabilized

plus

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

Make rs587777720(A;G)

Make rs587777720(G;G)

Reference

GRCh38 38.1/142

Chromosome

4

Position

154604986

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs587777720
dbSNP (classic)	rs587777720
ClinGen	rs587777720
ebi	rs587777720
HLI	rs587777720
Exac	rs587777720
Gnomad	rs587777720
Varsome	rs587777720
LitVar	rs587777720
Map	rs587777720
PheGenI	rs587777720
Biobank	rs587777720
1000 genomes	rs587777720
hgdp	rs587777720
ensembl	rs587777720
geneview	rs587777720
scholar	rs587777720
google	rs587777720
pharmgkb	rs587777720
gwascentral	rs587777720
openSNP	rs587777720
23andMe	rs587777720
SNPshot	rs587777720
SNPdbe	rs587777720
MSV3d	rs587777720
GWAS Ctlg	rs587777720

Max Magnitude

0

ClinVar
Risk	rs587777720(G;G)
Alt	rs587777720(G;G)
Reference	Rs587777720(A;A)
Significance	Pathogenic
Disease	Hypodysfibrinogenemia
Variation	info
Gene	FGG
CLNDBN	Hypodysfibrinogenemia
Reversed	0
HGVS	NC_000004.11:g.155526138A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000144152.3,