rs587776838

Orientation

plus

Stabilized

plus

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

Make rs587776838(C;T)

Make rs587776838(T;T)

Reference

GRCh38 38.1/142

Chromosome

4

Position

154612013

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs587776838
dbSNP (classic)	rs587776838
ClinGen	rs587776838
ebi	rs587776838
HLI	rs587776838
Exac	rs587776838
Gnomad	rs587776838
Varsome	rs587776838
LitVar	rs587776838
Map	rs587776838
PheGenI	rs587776838
Biobank	rs587776838
1000 genomes	rs587776838
hgdp	rs587776838
ensembl	rs587776838
geneview	rs587776838
scholar	rs587776838
google	rs587776838
pharmgkb	rs587776838
gwascentral	rs587776838
openSNP	rs587776838
23andMe	rs587776838
SNPshot	rs587776838
SNPdbe	rs587776838
MSV3d	rs587776838
GWAS Ctlg	rs587776838

Max Magnitude

0

ClinVar
Risk	rs587776838(T;T)
Alt	rs587776838(T;T)
Reference	Rs587776838(C;C)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	FGG
CLNDBN	Afibrinogenemia, congenital
Reversed	0
HGVS	NC_000004.11:g.155533165C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017799.28,