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rs137852452

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852452(C;T)
Make rs137852452(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154903951
GeneF8
is asnp
is mentioned by
dbSNPrs137852452
ebirs137852452
HLIrs137852452
Exacrs137852452
Varsomers137852452
Maprs137852452
PheGenIrs137852452
hapmaprs137852452
1000 genomesrs137852452
hgdprs137852452
ensemblrs137852452
gopubmedrs137852452
geneviewrs137852452
scholarrs137852452
googlers137852452
pharmgkbrs137852452
gwascentralrs137852452
openSNPrs137852452
23andMers137852452
23andMe allrs137852452
SNP Nexus

SNPshotrs137852452
SNPdbers137852452
MSV3drs137852452
GWAS Ctlgrs137852452
Max Magnitude0
OMIM306700
Desc
Variant0217
Relatedalso
ClinVar
Risk rs137852452(T;T)
Alt rs137852452(T;T)
Reference rs137852452(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.154132226G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011013.6,