Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906448

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs387906448(-;-)
Make rs387906448(-;AG)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154930827
GeneF8
is asnp
is mentioned by
dbSNPrs387906448
ebirs387906448
HLIrs387906448
Exacrs387906448
Varsomers387906448
Maprs387906448
PheGenIrs387906448
hapmaprs387906448
1000 genomesrs387906448
hgdprs387906448
ensemblrs387906448
gopubmedrs387906448
geneviewrs387906448
scholarrs387906448
googlers387906448
pharmgkbrs387906448
gwascentralrs387906448
openSNPrs387906448
23andMers387906448
23andMe allrs387906448
SNP Nexus

SNPshotrs387906448
SNPdbers387906448
MSV3drs387906448
GWAS Ctlgrs387906448
Max Magnitude0
ClinVar
Risk rs387906448(;)
Alt rs387906448(;)
Reference rs387906448(AG;AG)
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.154159102_154159103delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000010963.4,