rs137852257

Orientation

plus

Stabilized

plus

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

Make rs137852257(A;A)

Make rs137852257(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139561754

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852257
dbSNP (classic)	rs137852257
ClinGen	rs137852257
ebi	rs137852257
HLI	rs137852257
Exac	rs137852257
Gnomad	rs137852257
Varsome	rs137852257
LitVar	rs137852257
Map	rs137852257
PheGenI	rs137852257
Biobank	rs137852257
1000 genomes	rs137852257
hgdp	rs137852257
ensembl	rs137852257
geneview	rs137852257
scholar	rs137852257
google	rs137852257
pharmgkb	rs137852257
gwascentral	rs137852257
openSNP	rs137852257
23andMe	rs137852257
SNPshot	rs137852257
SNPdbe	rs137852257
MSV3d	rs137852257
GWAS Ctlg	rs137852257

Max Magnitude

0

OMIM	300746
Desc
Variant	0054
Related	also

ClinVar
Risk	rs137852257(A;A)
Alt	rs137852257(A;A)
Reference	Rs137852257(G;G)
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.138643913G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011357.7,