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rs137852436

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852436(A;A)
Make rs137852436(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154931623
GeneF8
is asnp
is mentioned by
dbSNPrs137852436
ebirs137852436
HLIrs137852436
Exacrs137852436
Varsomers137852436
Maprs137852436
PheGenIrs137852436
hapmaprs137852436
1000 genomesrs137852436
hgdprs137852436
ensemblrs137852436
gopubmedrs137852436
geneviewrs137852436
scholarrs137852436
googlers137852436
pharmgkbrs137852436
gwascentralrs137852436
openSNPrs137852436
23andMers137852436
23andMe allrs137852436
SNP Nexus

SNPshotrs137852436
SNPdbers137852436
MSV3drs137852436
GWAS Ctlgrs137852436
Max Magnitude0
OMIM306700
Desc
Variant0163
Relatedalso
ClinVar
Risk rs137852436(A;A)
Alt rs137852436(A;A)
Reference rs137852436(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.154159898C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010959.5,