rs1060499784

Orientation

minus

Stabilized

minus

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

Make rs1060499784(A;A)

Make rs1060499784(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

154930646

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs1060499784
dbSNP (classic)	rs1060499784
ClinGen	rs1060499784
ebi	rs1060499784
HLI	rs1060499784
Exac	rs1060499784
Gnomad	rs1060499784
Varsome	rs1060499784
LitVar	rs1060499784
Map	rs1060499784
PheGenI	rs1060499784
Biobank	rs1060499784
1000 genomes	rs1060499784
hgdp	rs1060499784
ensembl	rs1060499784
geneview	rs1060499784
scholar	rs1060499784
google	rs1060499784
pharmgkb	rs1060499784
gwascentral	rs1060499784
openSNP	rs1060499784
23andMe	rs1060499784
SNPshot	rs1060499784
SNPdbe	rs1060499784
MSV3d	rs1060499784
GWAS Ctlg	rs1060499784

Max Magnitude

0

ClinVar
Risk	rs1060499784(A;A)
Alt	rs1060499784(A;A)
Reference	Rs1060499784(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary factor VIII deficiency disease
Variation	info
Gene	F8
CLNDBN	Hereditary factor VIII deficiency disease
Reversed	1
HGVS	NC_000023.10:g.154158921C>T
CLNSRC
CLNACC	RCV000454124.1,