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rs137852471

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852471(C;T)
Make rs137852471(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154860467
GeneF8
is asnp
is mentioned by
dbSNPrs137852471
ebirs137852471
HLIrs137852471
Exacrs137852471
Varsomers137852471
Maprs137852471
PheGenIrs137852471
hapmaprs137852471
1000 genomesrs137852471
hgdprs137852471
ensemblrs137852471
gopubmedrs137852471
geneviewrs137852471
scholarrs137852471
googlers137852471
pharmgkbrs137852471
gwascentralrs137852471
openSNPrs137852471
23andMers137852471
23andMe allrs137852471
SNP Nexus

SNPshotrs137852471
SNPdbers137852471
MSV3drs137852471
GWAS Ctlgrs137852471
Max Magnitude0
OMIM306700
Desc
Variant0247
Relatedalso
ClinVar
Risk rs137852471(T;T)
Alt rs137852471(T;T)
Reference rs137852471(C;C)
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.154088742G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011043.5,