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rs137852474

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852474(A;A)
Make rs137852474(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154837685
GeneF8
is asnp
is mentioned by
dbSNPrs137852474
ebirs137852474
HLIrs137852474
Exacrs137852474
Varsomers137852474
Maprs137852474
PheGenIrs137852474
hapmaprs137852474
1000 genomesrs137852474
hgdprs137852474
ensemblrs137852474
gopubmedrs137852474
geneviewrs137852474
scholarrs137852474
googlers137852474
pharmgkbrs137852474
gwascentralrs137852474
openSNPrs137852474
23andMers137852474
23andMe allrs137852474
SNP Nexus

SNPshotrs137852474
SNPdbers137852474
MSV3drs137852474
GWAS Ctlgrs137852474
Max Magnitude0
OMIM306700
Desc
Variant0251
Relatedalso
ClinVar
Risk rs137852474(A;A)
Alt rs137852474(A;A)
Reference rs137852474(G;G)
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.154065960C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011047.5,