rs137852255

Orientation

plus

Stabilized

plus

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

Make rs137852255(C;C)

Make rs137852255(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139561743

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852255
dbSNP (classic)	rs137852255
ClinGen	rs137852255
ebi	rs137852255
HLI	rs137852255
Exac	rs137852255
Gnomad	rs137852255
Varsome	rs137852255
LitVar	rs137852255
Map	rs137852255
PheGenI	rs137852255
Biobank	rs137852255
1000 genomes	rs137852255
hgdp	rs137852255
ensembl	rs137852255
geneview	rs137852255
scholar	rs137852255
google	rs137852255
pharmgkb	rs137852255
gwascentral	rs137852255
openSNP	rs137852255
23andMe	rs137852255
SNPshot	rs137852255
SNPdbe	rs137852255
MSV3d	rs137852255
GWAS Ctlg	rs137852255

Max Magnitude

0

OMIM	300746
Desc
Variant	0051
Related	also

ClinVar
Risk	rs137852255(C;C)
Alt	rs137852255(C;C)
Reference	Rs137852255(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.138643902T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011354.6,