rs137852242

Orientation

plus

Stabilized

plus

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

Make rs137852242(G;T)

Make rs137852242(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139551220

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852242
dbSNP (classic)	rs137852242
ClinGen	rs137852242
ebi	rs137852242
HLI	rs137852242
Exac	rs137852242
Gnomad	rs137852242
Varsome	rs137852242
LitVar	rs137852242
Map	rs137852242
PheGenI	rs137852242
Biobank	rs137852242
1000 genomes	rs137852242
hgdp	rs137852242
ensembl	rs137852242
geneview	rs137852242
scholar	rs137852242
google	rs137852242
pharmgkb	rs137852242
gwascentral	rs137852242
openSNP	rs137852242
23andMe	rs137852242
SNPshot	rs137852242
SNPdbe	rs137852242
MSV3d	rs137852242
GWAS Ctlg	rs137852242

Max Magnitude

0

OMIM	300746
Desc
Variant	0032
Related	also

ClinVar
Risk	rs137852242(T;T)
Alt	rs137852242(T;T)
Reference	Rs137852242(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.138633379G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011338.6,