rs137852412

Orientation

minus

Stabilized

minus

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

Make rs137852412(A;G)

Make rs137852412(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154961137

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs137852412
dbSNP (classic)	rs137852412
ClinGen	rs137852412
ebi	rs137852412
HLI	rs137852412
Exac	rs137852412
Gnomad	rs137852412
Varsome	rs137852412
LitVar	rs137852412
Map	rs137852412
PheGenI	rs137852412
Biobank	rs137852412
1000 genomes	rs137852412
hgdp	rs137852412
ensembl	rs137852412
geneview	rs137852412
scholar	rs137852412
google	rs137852412
pharmgkb	rs137852412
gwascentral	rs137852412
openSNP	rs137852412
23andMe	rs137852412
SNPshot	rs137852412
SNPdbe	rs137852412
MSV3d	rs137852412
GWAS Ctlg	rs137852412

Merged from

Rs28937275

Max Magnitude

0

OMIM	306700
Desc
Variant	0132
Related	also

ClinVar
Risk	rs137852412(G;G)
Alt	rs137852412(G;G)
Reference	Rs137852412(A;A)
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.154189412T>C
CLNSRC
CLNACC