rs104894807

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;T)	3	hemophilia B if male; carrier if female
(T;T)	0	common in clinvar

Make rs104894807(C;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

139548404

Gene

F9

is a	snp
is	mentioned by
dbSNP	rs104894807
dbSNP (classic)	rs104894807
ClinGen	rs104894807
ebi	rs104894807
HLI	rs104894807
Exac	rs104894807
Gnomad	rs104894807
Varsome	rs104894807
LitVar	rs104894807
Map	rs104894807
PheGenI	rs104894807
Biobank	rs104894807
1000 genomes	rs104894807
hgdp	rs104894807
ensembl	rs104894807
geneview	rs104894807
scholar	rs104894807
google	rs104894807
pharmgkb	rs104894807
gwascentral	rs104894807
openSNP	rs104894807
23andMe	rs104894807
SNPshot	rs104894807
SNPdbe	rs104894807
MSV3d	rs104894807
GWAS Ctlg	rs104894807

Max Magnitude

3

OMIM	300746
Desc
Variant	0026
Related	also

ClinVar
Risk	rs104894807(C;C)
Alt	rs104894807(C;C)
Reference	Rs104894807(T;T)
Significance	Untested
Disease
Variation	info
Gene	F9
CLNDBN
Reversed	0
HGVS	NC_000023.10:g.138630563T>C
CLNSRC
CLNACC