rs146387238

Orientation

plus

Stabilized

plus

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

Make rs146387238(A;A)

Make rs146387238(A;C)

Reference

GRCh38 38.1/142

Chromosome

4

Position

154587511

Gene

FGA

is a	snp
is	mentioned by
dbSNP	rs146387238
dbSNP (classic)	rs146387238
ClinGen	rs146387238
ebi	rs146387238
HLI	rs146387238
Exac	rs146387238
Gnomad	rs146387238
Varsome	rs146387238
LitVar	rs146387238
Map	rs146387238
PheGenI	rs146387238
Biobank	rs146387238
1000 genomes	rs146387238
hgdp	rs146387238
ensembl	rs146387238
geneview	rs146387238
scholar	rs146387238
google	rs146387238
pharmgkb	rs146387238
gwascentral	rs146387238
openSNP	rs146387238
23andMe	rs146387238
SNPshot	rs146387238
SNPdbe	rs146387238
MSV3d	rs146387238
GWAS Ctlg	rs146387238

Max Magnitude

0

ClinVar
Risk	rs146387238(A;A) rs146387238(G;G)
Alt	rs146387238(A;A) rs146387238(G;G)
Reference	Rs146387238(C;C)
Significance	Pathogenic
Disease	Afibrinogenemia Hypodysfibrinogenemia
Variation	info
Gene	FGA
CLNDBN	Afibrinogenemia, congenital Hypodysfibrinogenemia, congenital
Reversed	0
HGVS	NC_000004.11:g.155508663C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017877.28, RCV000030942.28,