rs387906435

Orientation

minus

Stabilized

minus

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

Make rs387906435(-;-)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154996996

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs387906435
dbSNP (classic)	rs387906435
ClinGen	rs387906435
ebi	rs387906435
HLI	rs387906435
Exac	rs387906435
Gnomad	rs387906435
Varsome	rs387906435
LitVar	rs387906435
Map	rs387906435
PheGenI	rs387906435
Biobank	rs387906435
1000 genomes	rs387906435
hgdp	rs387906435
ensembl	rs387906435
geneview	rs387906435
scholar	rs387906435
google	rs387906435
pharmgkb	rs387906435
gwascentral	rs387906435
openSNP	rs387906435
23andMe	rs387906435
SNPshot	rs387906435
SNPdbe	rs387906435
MSV3d	rs387906435
GWAS Ctlg	rs387906435

Max Magnitude

3.5

ClinVar
Risk	rs387906435(-;-)
Alt	rs387906435(-;-)
Reference	Rs387906435(GT;GT)
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.154225271_154225272delAC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010873.6,