rs121964916

Orientation

minus

Stabilized

minus

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

Make rs121964916(A;A)

Make rs121964916(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

109760567

Gene

CFI

is a	snp
is	mentioned by
dbSNP	rs121964916
dbSNP (classic)	rs121964916
ClinGen	rs121964916
ebi	rs121964916
HLI	rs121964916
Exac	rs121964916
Gnomad	rs121964916
Varsome	rs121964916
LitVar	rs121964916
Map	rs121964916
PheGenI	rs121964916
Biobank	rs121964916
1000 genomes	rs121964916
hgdp	rs121964916
ensembl	rs121964916
geneview	rs121964916
scholar	rs121964916
google	rs121964916
pharmgkb	rs121964916
gwascentral	rs121964916
openSNP	rs121964916
23andMe	rs121964916
SNPshot	rs121964916
SNPdbe	rs121964916
MSV3d	rs121964916
GWAS Ctlg	rs121964916

Max Magnitude

0

OMIM	217030
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121964916(A;A)
Alt	rs121964916(A;A)
Reference	Rs121964916(G;G)
Significance	Pathogenic
Disease	Afibrinogenemia
Variation	info
Gene	CFI
CLNDBN	Afibrinogenemia
Reversed	1
HGVS	NC_000004.11:g.110681723C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012907.22,