rs137852226

Orientation

plus

Stabilized

plus

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

Make rs137852226(A;T)

Make rs137852226(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139537139

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852226
dbSNP (classic)	rs137852226
ClinGen	rs137852226
ebi	rs137852226
HLI	rs137852226
Exac	rs137852226
Gnomad	rs137852226
Varsome	rs137852226
LitVar	rs137852226
Map	rs137852226
PheGenI	rs137852226
Biobank	rs137852226
1000 genomes	rs137852226
hgdp	rs137852226
ensembl	rs137852226
geneview	rs137852226
scholar	rs137852226
google	rs137852226
pharmgkb	rs137852226
gwascentral	rs137852226
openSNP	rs137852226
23andMe	rs137852226
SNPshot	rs137852226
SNPdbe	rs137852226
MSV3d	rs137852226
GWAS Ctlg	rs137852226

Max Magnitude

0

OMIM	300746
Desc
Variant	0014
Related	also

ClinVar
Risk	rs137852226(T;T)
Alt	rs137852226(T;T)
Reference	Rs137852226(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.138619298A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011317.7,