rs137852266

Orientation

plus

Stabilized

plus

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

Make rs137852266(A;A)

Make rs137852266(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139561992

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852266
dbSNP (classic)	rs137852266
ClinGen	rs137852266
ebi	rs137852266
HLI	rs137852266
Exac	rs137852266
Gnomad	rs137852266
Varsome	rs137852266
LitVar	rs137852266
Map	rs137852266
PheGenI	rs137852266
Biobank	rs137852266
1000 genomes	rs137852266
hgdp	rs137852266
ensembl	rs137852266
geneview	rs137852266
scholar	rs137852266
google	rs137852266
pharmgkb	rs137852266
gwascentral	rs137852266
openSNP	rs137852266
23andMe	rs137852266
SNPshot	rs137852266
SNPdbe	rs137852266
MSV3d	rs137852266
GWAS Ctlg	rs137852266

Max Magnitude

0

OMIM	300746
Desc
Variant	0066
Related	also

OMIM	300746
Desc
Variant	0067
Related	also

ClinVar
Risk	rs137852266(A;A) rs137852266(T;T)
Alt	rs137852266(A;A) rs137852266(T;T)
Reference	Rs137852266(C;C)
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.138644151C>A; NC_000023.10:g.138644151C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011368.4, RCV000011369.5,