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rs137852440

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852440(A;A)
Make rs137852440(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154906488
GeneF8
is asnp
is mentioned by
dbSNPrs137852440
ebirs137852440
HLIrs137852440
Exacrs137852440
Varsomers137852440
Maprs137852440
PheGenIrs137852440
hapmaprs137852440
1000 genomesrs137852440
hgdprs137852440
ensemblrs137852440
gopubmedrs137852440
geneviewrs137852440
scholarrs137852440
googlers137852440
pharmgkbrs137852440
gwascentralrs137852440
openSNPrs137852440
23andMers137852440
23andMe allrs137852440
SNP Nexus

SNPshotrs137852440
SNPdbers137852440
MSV3drs137852440
GWAS Ctlgrs137852440
Max Magnitude0
OMIM306700
Desc
Variant0187
Relatedalso
ClinVar
Risk rs137852440(A;A)
Alt rs137852440(A;A)
Reference rs137852440(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.154134763C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010983.4,