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rs137852448

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852448(C;T)
Make rs137852448(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154904434
GeneF8
is asnp
is mentioned by
dbSNPrs137852448
ebirs137852448
HLIrs137852448
Exacrs137852448
Varsomers137852448
Maprs137852448
PheGenIrs137852448
hapmaprs137852448
1000 genomesrs137852448
hgdprs137852448
ensemblrs137852448
gopubmedrs137852448
geneviewrs137852448
scholarrs137852448
googlers137852448
pharmgkbrs137852448
gwascentralrs137852448
openSNPrs137852448
23andMers137852448
23andMe allrs137852448
SNP Nexus

SNPshotrs137852448
SNPdbers137852448
MSV3drs137852448
GWAS Ctlgrs137852448
Max Magnitude0
OMIM306700
Desc
Variant0208
Relatedalso
ClinVar
Risk rs137852448(T;T)
Alt rs137852448(T;T)
Reference rs137852448(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.154132709G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011004.4,