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rs137852424

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852424(C;T)
Make rs137852424(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154953991
GeneF8
is asnp
is mentioned by
dbSNPrs137852424
ebirs137852424
HLIrs137852424
Exacrs137852424
Varsomers137852424
Maprs137852424
PheGenIrs137852424
hapmaprs137852424
1000 genomesrs137852424
hgdprs137852424
ensemblrs137852424
gopubmedrs137852424
geneviewrs137852424
scholarrs137852424
googlers137852424
pharmgkbrs137852424
gwascentralrs137852424
openSNPrs137852424
23andMers137852424
23andMe allrs137852424
SNP Nexus

SNPshotrs137852424
SNPdbers137852424
MSV3drs137852424
GWAS Ctlgrs137852424
Max Magnitude0
OMIM306700
Desc
Variant0149
Relatedalso
ClinVar
Risk rs137852424(A,T;A,T)
Alt rs137852424(A,T;A,T)
Reference rs137852424(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.154182266G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010945.4,