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rs387906436

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs387906436(-;-)
Make rs387906436(-;AG)
Make rs387906436(AG;AG)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154984786
GeneF8
is asnp
is mentioned by
dbSNPrs387906436
ebirs387906436
HLIrs387906436
Exacrs387906436
Varsomers387906436
Maprs387906436
PheGenIrs387906436
hapmaprs387906436
1000 genomesrs387906436
hgdprs387906436
ensemblrs387906436
gopubmedrs387906436
geneviewrs387906436
scholarrs387906436
googlers387906436
pharmgkbrs387906436
gwascentralrs387906436
openSNPrs387906436
23andMers387906436
23andMe allrs387906436
SNP Nexus

SNPshotrs387906436
SNPdbers387906436
MSV3drs387906436
GWAS Ctlgrs387906436
Max Magnitude0
ClinVar
Risk rs387906436(;)
Alt rs387906436(;)
Reference rs387906436(GA;GA)
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.154213061_154213062delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000010894.4,