rs606231225

Orientation

minus

Stabilized

minus

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

Make rs606231225(-;T)

Make rs606231225(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

154586717

Gene

FGA

is a	snp
is	mentioned by
dbSNP	rs606231225
dbSNP (classic)	rs606231225
ClinGen	rs606231225
ebi	rs606231225
HLI	rs606231225
Exac	rs606231225
Gnomad	rs606231225
Varsome	rs606231225
LitVar	rs606231225
Map	rs606231225
PheGenI	rs606231225
Biobank	rs606231225
1000 genomes	rs606231225
hgdp	rs606231225
ensembl	rs606231225
geneview	rs606231225
scholar	rs606231225
google	rs606231225
pharmgkb	rs606231225
gwascentral	rs606231225
openSNP	rs606231225
23andMe	rs606231225
SNPshot	rs606231225
SNPdbe	rs606231225
MSV3d	rs606231225
GWAS Ctlg	rs606231225

Max Magnitude

0

ClinVar
Risk	rs606231225(T;T)
Alt	rs606231225(T;T)
Reference	Rs606231225(-;-)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	FGA
CLNDBN	Afibrinogenemia, congenital
Reversed	1
HGVS	NC_000004.11:g.155507870dupA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017879.24,