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

rs137852427

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852427(A;C)
Make rs137852427(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154953981
GeneF8
is asnp
is mentioned by
dbSNPrs137852427
ebirs137852427
HLIrs137852427
Exacrs137852427
Varsomers137852427
Maprs137852427
PheGenIrs137852427
hapmaprs137852427
1000 genomesrs137852427
hgdprs137852427
ensemblrs137852427
gopubmedrs137852427
geneviewrs137852427
scholarrs137852427
googlers137852427
pharmgkbrs137852427
gwascentralrs137852427
openSNPrs137852427
23andMers137852427
23andMe allrs137852427
SNP Nexus

SNPshotrs137852427
SNPdbers137852427
MSV3drs137852427
GWAS Ctlgrs137852427
Max Magnitude0
OMIM306700
Desc
Variant0152
Relatedalso
ClinVar
Risk rs137852427(C;C)
Alt rs137852427(C;C)
Reference rs137852427(A;A)
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.154182256T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010948.5,