rs137852414

Orientation

minus

Stabilized

minus

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

Make rs137852414(A;A)

Make rs137852414(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154961120

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs137852414
dbSNP (classic)	rs137852414
ClinGen	rs137852414
ebi	rs137852414
HLI	rs137852414
Exac	rs137852414
Gnomad	rs137852414
Varsome	rs137852414
LitVar	rs137852414
Map	rs137852414
PheGenI	rs137852414
Biobank	rs137852414
1000 genomes	rs137852414
hgdp	rs137852414
ensembl	rs137852414
geneview	rs137852414
scholar	rs137852414
google	rs137852414
pharmgkb	rs137852414
gwascentral	rs137852414
openSNP	rs137852414
23andMe	rs137852414
SNPshot	rs137852414
SNPdbe	rs137852414
MSV3d	rs137852414
GWAS Ctlg	rs137852414

Merged from

Rs28936969

Max Magnitude

0

OMIM	306700
Desc
Variant	0134
Related	also

ClinVar
Risk	rs137852414(A;A)
Alt	rs137852414(A;A)
Reference	Rs137852414(G;G)
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.154189395C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010930.7,