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rs137852447

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852447(A;T)
Make rs137852447(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154904861
GeneF8
is asnp
is mentioned by
dbSNPrs137852447
ebirs137852447
HLIrs137852447
Exacrs137852447
Varsomers137852447
Maprs137852447
PheGenIrs137852447
hapmaprs137852447
1000 genomesrs137852447
hgdprs137852447
ensemblrs137852447
gopubmedrs137852447
geneviewrs137852447
scholarrs137852447
googlers137852447
pharmgkbrs137852447
gwascentralrs137852447
openSNPrs137852447
23andMers137852447
23andMe allrs137852447
SNP Nexus

SNPshotrs137852447
SNPdbers137852447
MSV3drs137852447
GWAS Ctlgrs137852447
Max Magnitude0
OMIM306700
Desc
Variant0200
Relatedalso
ClinVar
Risk rs137852447(T;T)
Alt rs137852447(T;T)
Reference rs137852447(A;A)
Significance Probable-Pathogenic
Disease Hereditary factor VIII deficiency disease
Variation info
Gene F8
CLNDBN Hereditary factor VIII deficiency disease
Reversed 1
HGVS NC_000023.10:g.154133136T>A
CLNSRC
CLNACC