rs587776735

Orientation

plus

Stabilized

plus

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

Make rs587776735(C;C)

Make rs587776735(C;T)

Reference

GRCh38 38.1/142

Chromosome

X

Position

139537388

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs587776735
dbSNP (classic)	rs587776735
ClinGen	rs587776735
ebi	rs587776735
HLI	rs587776735
Exac	rs587776735
Gnomad	rs587776735
Varsome	rs587776735
LitVar	rs587776735
Map	rs587776735
PheGenI	rs587776735
Biobank	rs587776735
1000 genomes	rs587776735
hgdp	rs587776735
ensembl	rs587776735
geneview	rs587776735
scholar	rs587776735
google	rs587776735
pharmgkb	rs587776735
gwascentral	rs587776735
openSNP	rs587776735
23andMe	rs587776735
SNPshot	rs587776735
SNPdbe	rs587776735
MSV3d	rs587776735
GWAS Ctlg	rs587776735

Max Magnitude

0

ClinVar
Risk	rs587776735(C;C)
Alt	rs587776735(C;C)
Reference	Rs587776735(T;T)
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.138619547T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011409.5,