rs1057516616

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	5	Factor XI deficiency
(-;CATT)	3	carrier of factor XI mutation
(CATT;CATT)	0	common in clinvar

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

186267161

Gene

F11

is a	snp
is	mentioned by
dbSNP	rs1057516616
dbSNP (classic)	rs1057516616
ClinGen	rs1057516616
ebi	rs1057516616
HLI	rs1057516616
Exac	rs1057516616
Gnomad	rs1057516616
Varsome	rs1057516616
LitVar	rs1057516616
Map	rs1057516616
PheGenI	rs1057516616
Biobank	rs1057516616
1000 genomes	rs1057516616
hgdp	rs1057516616
ensembl	rs1057516616
geneview	rs1057516616
scholar	rs1057516616
google	rs1057516616
pharmgkb	rs1057516616
gwascentral	rs1057516616
openSNP	rs1057516616
23andMe	rs1057516616
SNPshot	rs1057516616
SNPdbe	rs1057516616
MSV3d	rs1057516616
GWAS Ctlg	rs1057516616

Max Magnitude

5

ClinVar
Risk	Rs1057516616(-;-)
Alt	Rs1057516616(-;-)
Reference	Rs1057516616(CATT;CATT)
Significance	Probable-Pathogenic
Disease	Hereditary factor XI deficiency disease
Variation	info
Gene	F11
CLNDBN	Hereditary factor XI deficiency disease
Reversed	0
HGVS	NC_000004.11:g.187188315_187188318delCATT
CLNSRC
CLNACC	RCV000411987.1,