rs1057517446

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	5	Factor XI deficiency
(CACT;CACT)	0	common in clinvar
(CTCA;CTCA)	0	common/normal

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

186284188

Gene

F11

is a	snp
is	mentioned by
dbSNP	rs1057517446
dbSNP (classic)	rs1057517446
ClinGen	rs1057517446
ebi	rs1057517446
HLI	rs1057517446
Exac	rs1057517446
Gnomad	rs1057517446
Varsome	rs1057517446
LitVar	rs1057517446
Map	rs1057517446
PheGenI	rs1057517446
Biobank	rs1057517446
1000 genomes	rs1057517446
hgdp	rs1057517446
ensembl	rs1057517446
geneview	rs1057517446
scholar	rs1057517446
google	rs1057517446
pharmgkb	rs1057517446
gwascentral	rs1057517446
openSNP	rs1057517446
23andMe	rs1057517446
SNPshot	rs1057517446
SNPdbe	rs1057517446
MSV3d	rs1057517446
GWAS Ctlg	rs1057517446

Max Magnitude

5

ClinVar
Risk	Rs1057517446(-;-)
Alt	Rs1057517446(-;-)
Reference	Rs1057517446(CACT;CACT)
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.187205342_187205345delCTCA
CLNSRC
CLNACC	RCV000411516.1,