rs137852264

Orientation

plus

Stabilized

plus

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

Make rs137852264(G;T)

Make rs137852264(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139561911

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852264
dbSNP (classic)	rs137852264
ClinGen	rs137852264
ebi	rs137852264
HLI	rs137852264
Exac	rs137852264
Gnomad	rs137852264
Varsome	rs137852264
LitVar	rs137852264
Map	rs137852264
PheGenI	rs137852264
Biobank	rs137852264
1000 genomes	rs137852264
hgdp	rs137852264
ensembl	rs137852264
geneview	rs137852264
scholar	rs137852264
google	rs137852264
pharmgkb	rs137852264
gwascentral	rs137852264
openSNP	rs137852264
23andMe	rs137852264
SNPshot	rs137852264
SNPdbe	rs137852264
MSV3d	rs137852264
GWAS Ctlg	rs137852264

Max Magnitude

0

OMIM	300746
Desc
Variant	0062
Related	also

ClinVar
Risk	rs137852264(T;T)
Alt	rs137852264(T;T)
Reference	Rs137852264(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.138644070G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011364.3,