rs587776736

Orientation

plus

Stabilized

plus

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

Make rs587776736(-;-)

Make rs587776736(-;AG)

Reference

GRCh38 38.1/142

Chromosome

X

Position

139551081

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs587776736
dbSNP (classic)	rs587776736
ClinGen	rs587776736
ebi	rs587776736
HLI	rs587776736
Exac	rs587776736
Gnomad	rs587776736
Varsome	rs587776736
LitVar	rs587776736
Map	rs587776736
PheGenI	rs587776736
Biobank	rs587776736
1000 genomes	rs587776736
hgdp	rs587776736
ensembl	rs587776736
geneview	rs587776736
scholar	rs587776736
google	rs587776736
pharmgkb	rs587776736
gwascentral	rs587776736
openSNP	rs587776736
23andMe	rs587776736
SNPshot	rs587776736
SNPdbe	rs587776736
MSV3d	rs587776736
GWAS Ctlg	rs587776736

Max Magnitude

0

ClinVar
Risk	rs587776736(-;-)
Alt	rs587776736(-;-)
Reference	Rs587776736(AG;AG)
Significance	Pathogenic
Disease	Hereditary factor IX deficiency disease
Variation	info
Gene	F9
CLNDBN	Hereditary factor IX deficiency disease
Reversed	0
HGVS	NC_000023.10:g.138633240_138633241delAG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011412.5,