rs387906453

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(TCTTC;TCTTC)	0	common in clinvar
(TTCTC;TTCTC)	0	common in clinvar

Make rs387906453(-;-)

Make rs387906453(-;CTCTT)

Make rs387906453(CTCTT;CTCTT)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154929493

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs387906453
dbSNP (classic)	rs387906453
ClinGen	rs387906453
ebi	rs387906453
HLI	rs387906453
Exac	rs387906453
Gnomad	rs387906453
Varsome	rs387906453
LitVar	rs387906453
Map	rs387906453
PheGenI	rs387906453
Biobank	rs387906453
1000 genomes	rs387906453
hgdp	rs387906453
ensembl	rs387906453
geneview	rs387906453
scholar	rs387906453
google	rs387906453
pharmgkb	rs387906453
gwascentral	rs387906453
openSNP	rs387906453
23andMe	rs387906453
SNPshot	rs387906453
SNPdbe	rs387906453
MSV3d	rs387906453
GWAS Ctlg	rs387906453

Max Magnitude

0

ClinVar
Risk	rs387906453(-;-)
Alt	rs387906453(-;-)
Reference	Rs387906453(TTCTC;TTCTC)
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.154157768_154157772delAAGAG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010971.3,