rs387906437

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;T)	3.5	Carrier of a Hemophilia A mutation
(T;T)	0	common in clinvar

Make rs387906437(-;-)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154969491

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs387906437
dbSNP (classic)	rs387906437
ClinGen	rs387906437
ebi	rs387906437
HLI	rs387906437
Exac	rs387906437
Gnomad	rs387906437
Varsome	rs387906437
LitVar	rs387906437
Map	rs387906437
PheGenI	rs387906437
Biobank	rs387906437
1000 genomes	rs387906437
hgdp	rs387906437
ensembl	rs387906437
geneview	rs387906437
scholar	rs387906437
google	rs387906437
pharmgkb	rs387906437
gwascentral	rs387906437
openSNP	rs387906437
23andMe	rs387906437
SNPshot	rs387906437
SNPdbe	rs387906437
MSV3d	rs387906437
GWAS Ctlg	rs387906437

Max Magnitude

3.5

ClinVar
Risk	rs387906437(-;-)
Alt	rs387906437(-;-)
Reference	Rs387906437(T;T)
Significance	Pathogenic
Disease	Hereditary factor VIII deficiency disease
Variation	info
Gene	F8
CLNDBN	Hereditary factor VIII deficiency disease
Reversed	1
HGVS	NC_000023.10:g.154197766delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010901.3,