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

rs137852394

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852394(A;A)
Make rs137852394(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154992996
GeneF8
is asnp
is mentioned by
dbSNPrs137852394
ebirs137852394
HLIrs137852394
Exacrs137852394
Varsomers137852394
Maprs137852394
PheGenIrs137852394
hapmaprs137852394
1000 genomesrs137852394
hgdprs137852394
ensemblrs137852394
gopubmedrs137852394
geneviewrs137852394
scholarrs137852394
googlers137852394
pharmgkbrs137852394
gwascentralrs137852394
openSNPrs137852394
23andMers137852394
23andMe allrs137852394
SNP Nexus

SNPshotrs137852394
SNPdbers137852394
MSV3drs137852394
GWAS Ctlgrs137852394
Max Magnitude0
OMIM306700
Desc
Variant0094
Relatedalso
ClinVar
Risk rs137852394(A;A)
Alt rs137852394(A;A)
Reference rs137852394(G;G)
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.154221271C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010890.5,