rs121913096

Orientation

minus

Stabilized

minus

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

Make rs121913096(A;A)

Make rs121913096(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154606908

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs121913096
dbSNP (classic)	rs121913096
ClinGen	rs121913096
ebi	rs121913096
HLI	rs121913096
Exac	rs121913096
Gnomad	rs121913096
Varsome	rs121913096
LitVar	rs121913096
Map	rs121913096
PheGenI	rs121913096
Biobank	rs121913096
1000 genomes	rs121913096
hgdp	rs121913096
ensembl	rs121913096
geneview	rs121913096
scholar	rs121913096
google	rs121913096
pharmgkb	rs121913096
gwascentral	rs121913096
openSNP	rs121913096
23andMe	rs121913096
SNPshot	rs121913096
SNPdbe	rs121913096
MSV3d	rs121913096
GWAS Ctlg	rs121913096

Max Magnitude

0

OMIM	134850
Desc
Variant	0019
Related	also

ClinVar
Risk	rs121913096(A;A)
Alt	rs121913096(A;A)
Reference	Rs121913096(G;G)
Significance	Other
Disease	FIBRINOGEN HILLSBOROUGH
Variation	info
Gene	FGG
CLNDBN	FIBRINOGEN HILLSBOROUGH
Reversed	1
HGVS	NC_000004.11:g.155528060C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017801.2,