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rs137852433

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852433(C;T)
Make rs137852433(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154947823
GeneF8
is asnp
is mentioned by
dbSNPrs137852433
ebirs137852433
HLIrs137852433
Exacrs137852433
Varsomers137852433
Maprs137852433
PheGenIrs137852433
hapmaprs137852433
1000 genomesrs137852433
hgdprs137852433
ensemblrs137852433
gopubmedrs137852433
geneviewrs137852433
scholarrs137852433
googlers137852433
pharmgkbrs137852433
gwascentralrs137852433
openSNPrs137852433
23andMers137852433
23andMe allrs137852433
SNP Nexus

SNPshotrs137852433
SNPdbers137852433
MSV3drs137852433
GWAS Ctlgrs137852433
Max Magnitude0
OMIM306700
Desc
Variant0159
Relatedalso
ClinVar
Risk rs137852433(T;T)
Alt rs137852433(T;T)
Reference rs137852433(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.154176098G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010955.4,