rs137852273

Orientation

plus

Stabilized

plus

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

Make rs137852273(C;C)

Make rs137852273(C;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139561872

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852273
dbSNP (classic)	rs137852273
ClinGen	rs137852273
ebi	rs137852273
HLI	rs137852273
Exac	rs137852273
Gnomad	rs137852273
Varsome	rs137852273
LitVar	rs137852273
Map	rs137852273
PheGenI	rs137852273
Biobank	rs137852273
1000 genomes	rs137852273
hgdp	rs137852273
ensembl	rs137852273
geneview	rs137852273
scholar	rs137852273
google	rs137852273
pharmgkb	rs137852273
gwascentral	rs137852273
openSNP	rs137852273
23andMe	rs137852273
SNPshot	rs137852273
SNPdbe	rs137852273
MSV3d	rs137852273
GWAS Ctlg	rs137852273

Max Magnitude

0

OMIM	300746
Desc
Variant	0086
Related	also

ClinVar
Risk	rs137852273(C;C)
Alt	rs137852273(C;C)
Reference	Rs137852273(G;G)
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.138644031G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011388.2,