rs137852227

Orientation

plus

Stabilized

plus

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

Make rs137852227(C;T)

Make rs137852227(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139537144

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852227
dbSNP (classic)	rs137852227
ClinGen	rs137852227
ebi	rs137852227
HLI	rs137852227
Exac	rs137852227
Gnomad	rs137852227
Varsome	rs137852227
LitVar	rs137852227
Map	rs137852227
PheGenI	rs137852227
Biobank	rs137852227
1000 genomes	rs137852227
hgdp	rs137852227
ensembl	rs137852227
geneview	rs137852227
scholar	rs137852227
google	rs137852227
pharmgkb	rs137852227
gwascentral	rs137852227
openSNP	rs137852227
23andMe	rs137852227
SNPshot	rs137852227
SNPdbe	rs137852227
MSV3d	rs137852227
GWAS Ctlg	rs137852227

Max Magnitude

0

OMIM	300746
Desc
Variant	0015
Related	also

ClinVar
Risk	rs137852227(T;T)
Alt	rs137852227(T;T)
Reference	Rs137852227(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.138619303C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011318.3,