rs137852282

Orientation

plus

Stabilized

plus

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

Make rs137852282(C;C)

Make rs137852282(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139561854

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852282
dbSNP (classic)	rs137852282
ClinGen	rs137852282
ebi	rs137852282
HLI	rs137852282
Exac	rs137852282
Gnomad	rs137852282
Varsome	rs137852282
LitVar	rs137852282
Map	rs137852282
PheGenI	rs137852282
Biobank	rs137852282
1000 genomes	rs137852282
hgdp	rs137852282
ensembl	rs137852282
geneview	rs137852282
scholar	rs137852282
google	rs137852282
pharmgkb	rs137852282
gwascentral	rs137852282
openSNP	rs137852282
23andMe	rs137852282
SNPshot	rs137852282
SNPdbe	rs137852282
MSV3d	rs137852282
GWAS Ctlg	rs137852282

Max Magnitude

0

OMIM	300746
Desc
Variant	0108
Related	also

ClinVar
Risk	rs137852282(C;C)
Alt	rs137852282(C;C)
Reference	Rs137852282(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.138644013T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011410.4,