rs1057517151

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	5	Factor XI deficiency
(G;G)	0	common in clinvar

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

186273143

Gene

F11

is a	snp
is	mentioned by
dbSNP	rs1057517151
dbSNP (classic)	rs1057517151
ClinGen	rs1057517151
ebi	rs1057517151
HLI	rs1057517151
Exac	rs1057517151
Gnomad	rs1057517151
Varsome	rs1057517151
LitVar	rs1057517151
Map	rs1057517151
PheGenI	rs1057517151
Biobank	rs1057517151
1000 genomes	rs1057517151
hgdp	rs1057517151
ensembl	rs1057517151
geneview	rs1057517151
scholar	rs1057517151
google	rs1057517151
pharmgkb	rs1057517151
gwascentral	rs1057517151
openSNP	rs1057517151
23andMe	rs1057517151
SNPshot	rs1057517151
SNPdbe	rs1057517151
MSV3d	rs1057517151
GWAS Ctlg	rs1057517151

Max Magnitude

5

ClinVar
Risk	Rs1057517151(-;-)
Alt	Rs1057517151(-;-)
Reference	Rs1057517151(G;G)
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.187194297delG
CLNSRC
CLNACC	RCV000409581.1,