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rs387906434

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTGT;TTGT) 0 common in clinvar
(TTTG;TTTG) 0 common in clinvar
Make rs387906434(-;-)
Make rs387906434(-;GTTT)
Make rs387906434(GTTT;GTTT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154999534
GeneF8
is asnp
is mentioned by
dbSNPrs387906434
ebirs387906434
HLIrs387906434
Exacrs387906434
Varsomers387906434
Maprs387906434
PheGenIrs387906434
hapmaprs387906434
1000 genomesrs387906434
hgdprs387906434
ensemblrs387906434
gopubmedrs387906434
geneviewrs387906434
scholarrs387906434
googlers387906434
pharmgkbrs387906434
gwascentralrs387906434
openSNPrs387906434
23andMers387906434
23andMe allrs387906434
SNP Nexus

SNPshotrs387906434
SNPdbers387906434
MSV3drs387906434
GWAS Ctlgrs387906434
Max Magnitude0
ClinVar
Risk rs387906434(;)
Alt rs387906434(;)
Reference rs387906434(TTGT;TTGT)
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.154227809_154227812delAAAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000010872.2,