rs137852223

Orientation

plus

Stabilized

plus

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

Make rs137852223(C;T)

Make rs137852223(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139537090

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs137852223
dbSNP (classic)	rs137852223
ClinGen	rs137852223
ebi	rs137852223
HLI	rs137852223
Exac	rs137852223
Gnomad	rs137852223
Varsome	rs137852223
LitVar	rs137852223
Map	rs137852223
PheGenI	rs137852223
Biobank	rs137852223
1000 genomes	rs137852223
hgdp	rs137852223
ensembl	rs137852223
geneview	rs137852223
scholar	rs137852223
google	rs137852223
pharmgkb	rs137852223
gwascentral	rs137852223
openSNP	rs137852223
23andMe	rs137852223
SNPshot	rs137852223
SNPdbe	rs137852223
MSV3d	rs137852223
GWAS Ctlg	rs137852223

Max Magnitude

0

OMIM	300746
Desc
Variant	0011
Related	also

ClinVar
Risk	rs137852223(T;T)
Alt	rs137852223(T;T)
Reference	Rs137852223(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.138619249C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011313.4,