rs137852254

Orientation

plus

Stabilized

plus

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

Make rs137852254(C;T)

Make rs137852254(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139561710

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852254
dbSNP (classic)	rs137852254
ClinGen	rs137852254
ebi	rs137852254
HLI	rs137852254
Exac	rs137852254
Gnomad	rs137852254
Varsome	rs137852254
LitVar	rs137852254
Map	rs137852254
PheGenI	rs137852254
Biobank	rs137852254
1000 genomes	rs137852254
hgdp	rs137852254
ensembl	rs137852254
geneview	rs137852254
scholar	rs137852254
google	rs137852254
pharmgkb	rs137852254
gwascentral	rs137852254
openSNP	rs137852254
23andMe	rs137852254
SNPshot	rs137852254
SNPdbe	rs137852254
MSV3d	rs137852254
GWAS Ctlg	rs137852254

Max Magnitude

0

OMIM	300746
Desc
Variant	0050
Related	also

ClinVar
Risk	rs137852254(T;T)
Alt	rs137852254(T;T)
Reference	Rs137852254(C;C)
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.138643869C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011353.7,