rs387906506

Orientation

plus

Stabilized

plus

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

Make rs387906506(-;-)

Make rs387906506(-;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

113147444

Gene

F10

is a	snp
is	mentioned by
dbSNP	rs387906506
dbSNP (classic)	rs387906506
ClinGen	rs387906506
ebi	rs387906506
HLI	rs387906506
Exac	rs387906506
Gnomad	rs387906506
Varsome	rs387906506
LitVar	rs387906506
Map	rs387906506
PheGenI	rs387906506
Biobank	rs387906506
1000 genomes	rs387906506
hgdp	rs387906506
ensembl	rs387906506
geneview	rs387906506
scholar	rs387906506
google	rs387906506
pharmgkb	rs387906506
gwascentral	rs387906506
openSNP	rs387906506
23andMe	rs387906506
SNPshot	rs387906506
SNPdbe	rs387906506
MSV3d	rs387906506
GWAS Ctlg	rs387906506

Max Magnitude

0

ClinVar
Risk	rs387906506(-;-)
Alt	rs387906506(-;-)
Reference	Rs387906506(C;C)
Significance	Pathogenic
Disease	Factor X deficiency
Variation	info
Gene	F10
CLNDBN	Factor X deficiency
Reversed	0
HGVS	NC_000013.10:g.113801758delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012834.4,