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rs137852446

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852446(C;T)
Make rs137852446(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154904954
GeneF8
is asnp
is mentioned by
dbSNPrs137852446
ebirs137852446
HLIrs137852446
Exacrs137852446
Varsomers137852446
Maprs137852446
PheGenIrs137852446
hapmaprs137852446
1000 genomesrs137852446
hgdprs137852446
ensemblrs137852446
gopubmedrs137852446
geneviewrs137852446
scholarrs137852446
googlers137852446
pharmgkbrs137852446
gwascentralrs137852446
openSNPrs137852446
23andMers137852446
23andMe allrs137852446
SNP Nexus

SNPshotrs137852446
SNPdbers137852446
MSV3drs137852446
GWAS Ctlgrs137852446
Max Magnitude0
OMIM306700
Desc
Variant0196
Relatedalso
ClinVar
Risk rs137852446(T;T)
Alt rs137852446(T;T)
Reference rs137852446(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.154133229G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010992.4,