rs121964912

Orientation

minus

Stabilized

minus

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

Make rs121964912(A;T)

Make rs121964912(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

109746398

Gene

CFI

is a	snp
is	mentioned by
dbSNP	rs121964912
dbSNP (classic)	rs121964912
ClinGen	rs121964912
ebi	rs121964912
HLI	rs121964912
Exac	rs121964912
Gnomad	rs121964912
Varsome	rs121964912
LitVar	rs121964912
Map	rs121964912
PheGenI	rs121964912
Biobank	rs121964912
1000 genomes	rs121964912
hgdp	rs121964912
ensembl	rs121964912
geneview	rs121964912
scholar	rs121964912
google	rs121964912
pharmgkb	rs121964912
gwascentral	rs121964912
openSNP	rs121964912
23andMe	rs121964912
SNPshot	rs121964912
SNPdbe	rs121964912
MSV3d	rs121964912
GWAS Ctlg	rs121964912

Max Magnitude

0

OMIM	217030
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121964912(T;T)
Alt	rs121964912(T;T)
Reference	Rs121964912(A;A)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	CFI
CLNDBN	Afibrinogenemia
Reversed	1
HGVS	NC_000004.11:g.110667554T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012901.16,