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rs137852454

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852454(A;G)
Make rs137852454(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154902053
GeneF8
is asnp
is mentioned by
dbSNPrs137852454
ebirs137852454
HLIrs137852454
Exacrs137852454
Varsomers137852454
Maprs137852454
PheGenIrs137852454
hapmaprs137852454
1000 genomesrs137852454
hgdprs137852454
ensemblrs137852454
gopubmedrs137852454
geneviewrs137852454
scholarrs137852454
googlers137852454
pharmgkbrs137852454
gwascentralrs137852454
openSNPrs137852454
23andMers137852454
23andMe allrs137852454
SNP Nexus

SNPshotrs137852454
SNPdbers137852454
MSV3drs137852454
GWAS Ctlgrs137852454
Max Magnitude0
OMIM306700
Desc
Variant0222
Relatedalso
ClinVar
Risk rs137852454(G;G)
Alt rs137852454(G;G)
Reference rs137852454(A;A)
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.154130328T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011018.4,