rs137852382

Orientation

minus

Stabilized

minus

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

Make rs137852382(A;A)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154997065

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs137852382
dbSNP (classic)	rs137852382
ClinGen	rs137852382
ebi	rs137852382
HLI	rs137852382
Exac	rs137852382
Gnomad	rs137852382
Varsome	rs137852382
LitVar	rs137852382
Map	rs137852382
PheGenI	rs137852382
Biobank	rs137852382
1000 genomes	rs137852382
hgdp	rs137852382
ensembl	rs137852382
geneview	rs137852382
scholar	rs137852382
google	rs137852382
pharmgkb	rs137852382
gwascentral	rs137852382
openSNP	rs137852382
23andMe	rs137852382
SNPshot	rs137852382
SNPdbe	rs137852382
MSV3d	rs137852382
GWAS Ctlg	rs137852382

Merged from

Rs28935205

Max Magnitude

3.5

OMIM	306700
Desc
Variant	0082
Related	also

ClinVar
Risk	rs137852382(A;A)
Alt	rs137852382(A;A)
Reference	Rs137852382(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.154225340A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010878.3,