rs137852261

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3.5	Carrier of a Hemophilia B mutation
(T;T)	5.5	Hemophilia B (severity varies)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139561835

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852261
dbSNP (classic)	rs137852261
ClinGen	rs137852261
ebi	rs137852261
HLI	rs137852261
Exac	rs137852261
Gnomad	rs137852261
Varsome	rs137852261
LitVar	rs137852261
Map	rs137852261
PheGenI	rs137852261
Biobank	rs137852261
1000 genomes	rs137852261
hgdp	rs137852261
ensembl	rs137852261
geneview	rs137852261
scholar	rs137852261
google	rs137852261
pharmgkb	rs137852261
gwascentral	rs137852261
openSNP	rs137852261
23andMe	rs137852261
SNPshot	rs137852261
SNPdbe	rs137852261
MSV3d	rs137852261
GWAS Ctlg	rs137852261

Max Magnitude

5.5

OMIM	300746
Desc
Variant	0058
Related	also

ClinVar
Risk	rs137852261(A;A) Rs137852261(T;T)
Alt	rs137852261(A;A) Rs137852261(T;T)
Reference	Rs137852261(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.138643994C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011361.4,