rs587776839

Orientation

plus

Stabilized

plus

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

Make rs587776839(A;A)

Make rs587776839(A;T)

Reference

GRCh38 38.1/142

Chromosome

4

Position

154608970

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs587776839
dbSNP (classic)	rs587776839
ClinGen	rs587776839
ebi	rs587776839
HLI	rs587776839
Exac	rs587776839
Gnomad	rs587776839
Varsome	rs587776839
LitVar	rs587776839
Map	rs587776839
PheGenI	rs587776839
Biobank	rs587776839
1000 genomes	rs587776839
hgdp	rs587776839
ensembl	rs587776839
geneview	rs587776839
scholar	rs587776839
google	rs587776839
pharmgkb	rs587776839
gwascentral	rs587776839
openSNP	rs587776839
23andMe	rs587776839
SNPshot	rs587776839
SNPdbe	rs587776839
MSV3d	rs587776839
GWAS Ctlg	rs587776839

Max Magnitude

0

ClinVar
Risk	rs587776839(A;A)
Alt	rs587776839(A;A)
Reference	Rs587776839(T;T)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	FGG
CLNDBN	Afibrinogenemia, congenital
Reversed	0
HGVS	NC_000004.11:g.155530122T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017802.28,