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rs137852373

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852373(A;A)
Make rs137852373(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154928623
GeneF8
is asnp
is mentioned by
dbSNPrs137852373
ebirs137852373
HLIrs137852373
Exacrs137852373
Varsomers137852373
Maprs137852373
PheGenIrs137852373
hapmaprs137852373
1000 genomesrs137852373
hgdprs137852373
ensemblrs137852373
gopubmedrs137852373
geneviewrs137852373
scholarrs137852373
googlers137852373
pharmgkbrs137852373
gwascentralrs137852373
openSNPrs137852373
23andMers137852373
23andMe allrs137852373
SNP Nexus

SNPshotrs137852373
SNPdbers137852373
MSV3drs137852373
GWAS Ctlgrs137852373
Max Magnitude0
OMIM306700
Desc
Variant0063
Relatedalso
ClinVar
Risk rs137852373(A;A)
Alt rs137852373(A;A)
Reference rs137852373(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.154156898C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010859.2,