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rs137852431

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852431(A;A)
Make rs137852431(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154947854
GeneF8
is asnp
is mentioned by
dbSNPrs137852431
ebirs137852431
HLIrs137852431
Exacrs137852431
Varsomers137852431
Maprs137852431
PheGenIrs137852431
hapmaprs137852431
1000 genomesrs137852431
hgdprs137852431
ensemblrs137852431
gopubmedrs137852431
geneviewrs137852431
scholarrs137852431
googlers137852431
pharmgkbrs137852431
gwascentralrs137852431
openSNPrs137852431
23andMers137852431
23andMe allrs137852431
SNP Nexus

SNPshotrs137852431
SNPdbers137852431
MSV3drs137852431
GWAS Ctlgrs137852431
Max Magnitude0
OMIM306700
Desc
Variant0157
Relatedalso
ClinVar
Risk rs137852431(A;A)
Alt rs137852431(A;A)
Reference rs137852431(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.154176129C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010953.5,