rs137852234

Orientation

plus

Stabilized

plus

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

Reference

GRCh38 38.1/141

Chromosome

X

Position

139541127

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852234
dbSNP (classic)	rs137852234
ClinGen	rs137852234
ebi	rs137852234
HLI	rs137852234
Exac	rs137852234
Gnomad	rs137852234
Varsome	rs137852234
LitVar	rs137852234
Map	rs137852234
PheGenI	rs137852234
Biobank	rs137852234
1000 genomes	rs137852234
hgdp	rs137852234
ensembl	rs137852234
geneview	rs137852234
scholar	rs137852234
google	rs137852234
pharmgkb	rs137852234
gwascentral	rs137852234
openSNP	rs137852234
23andMe	rs137852234
SNPshot	rs137852234
SNPdbe	rs137852234
MSV3d	rs137852234
GWAS Ctlg	rs137852234

Max Magnitude

5.5

OMIM	300746
Desc
Variant	0023
Related	also

ClinVar
Risk	Rs137852234(G;G)
Alt	Rs137852234(G;G)
Reference	Rs137852234(A;A)
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.138623286A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011326.4,