rs137852224

Orientation

plus

Stabilized

plus

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

Make rs137852224(C;C)

Make rs137852224(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139537111

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852224
dbSNP (classic)	rs137852224
ClinGen	rs137852224
ebi	rs137852224
HLI	rs137852224
Exac	rs137852224
Gnomad	rs137852224
Varsome	rs137852224
LitVar	rs137852224
Map	rs137852224
PheGenI	rs137852224
Biobank	rs137852224
1000 genomes	rs137852224
hgdp	rs137852224
ensembl	rs137852224
geneview	rs137852224
scholar	rs137852224
google	rs137852224
pharmgkb	rs137852224
gwascentral	rs137852224
openSNP	rs137852224
23andMe	rs137852224
SNPshot	rs137852224
SNPdbe	rs137852224
MSV3d	rs137852224
GWAS Ctlg	rs137852224

Max Magnitude

0

OMIM	300746
Desc
Variant	0012
Related	also

ClinVar
Risk	rs137852224(C;C)
Alt	rs137852224(C;C)
Reference	Rs137852224(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.138619270T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011314.6,