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rs387906453

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCTTC;TCTTC) 0 common in clinvar
(TTCTC;TTCTC) 0 common in clinvar
Make rs387906453(-;-)
Make rs387906453(-;CTCTT)
Make rs387906453(CTCTT;CTCTT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154929493
GeneF8
is asnp
is mentioned by
dbSNPrs387906453
ebirs387906453
HLIrs387906453
Exacrs387906453
Varsomers387906453
Maprs387906453
PheGenIrs387906453
hapmaprs387906453
1000 genomesrs387906453
hgdprs387906453
ensemblrs387906453
gopubmedrs387906453
geneviewrs387906453
scholarrs387906453
googlers387906453
pharmgkbrs387906453
gwascentralrs387906453
openSNPrs387906453
23andMers387906453
23andMe allrs387906453
SNP Nexus

SNPshotrs387906453
SNPdbers387906453
MSV3drs387906453
GWAS Ctlgrs387906453
Max Magnitude0
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,