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rs137852439

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852439(C;T)
Make rs137852439(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154928647
GeneF8
is asnp
is mentioned by
dbSNPrs137852439
ebirs137852439
HLIrs137852439
Exacrs137852439
Varsomers137852439
Maprs137852439
PheGenIrs137852439
hapmaprs137852439
1000 genomesrs137852439
hgdprs137852439
ensemblrs137852439
gopubmedrs137852439
geneviewrs137852439
scholarrs137852439
googlers137852439
pharmgkbrs137852439
gwascentralrs137852439
openSNPrs137852439
23andMers137852439
23andMe allrs137852439
SNP Nexus

SNPshotrs137852439
SNPdbers137852439
MSV3drs137852439
GWAS Ctlgrs137852439
Max Magnitude0
OMIM306700
Desc
Variant0184
Relatedalso
OMIM306700
Desc
Variant0185
Relatedalso
ClinVar
Risk rs137852439(A,G,T;A,G,T)
Alt rs137852439(A,G,T;A,G,T)
Reference rs137852439(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.154156922G>A; NC_000023.10:g.154156922G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010980.6, RCV000010981.2,