rs755117226

Orientation

plus

Stabilized

plus

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

Make rs755117226(A;A)

Make rs755117226(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

154587520

Gene

FGA

is a	snp
is	mentioned by
dbSNP	rs755117226
dbSNP (classic)	rs755117226
ClinGen	rs755117226
ebi	rs755117226
HLI	rs755117226
Exac	rs755117226
Gnomad	rs755117226
Varsome	rs755117226
LitVar	rs755117226
Map	rs755117226
PheGenI	rs755117226
Biobank	rs755117226
1000 genomes	rs755117226
hgdp	rs755117226
ensembl	rs755117226
geneview	rs755117226
scholar	rs755117226
google	rs755117226
pharmgkb	rs755117226
gwascentral	rs755117226
openSNP	rs755117226
23andMe	rs755117226
SNPshot	rs755117226
SNPdbe	rs755117226
MSV3d	rs755117226
GWAS Ctlg	rs755117226

Max Magnitude

0

ClinVar
Risk	rs755117226(A;A)
Alt	rs755117226(A;A)
Reference	Rs755117226(G;G)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	FGA
CLNDBN	Afibrinogenemia, congenital
Reversed	0
HGVS	NC_000004.11:g.155508672G>A
CLNSRC
CLNACC	RCV000454272.1,