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rs137852423

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852423(C;C)
Make rs137852423(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154954009
GeneF8
is asnp
is mentioned by
dbSNPrs137852423
ebirs137852423
HLIrs137852423
Exacrs137852423
Varsomers137852423
Maprs137852423
PheGenIrs137852423
hapmaprs137852423
1000 genomesrs137852423
hgdprs137852423
ensemblrs137852423
gopubmedrs137852423
geneviewrs137852423
scholarrs137852423
googlers137852423
pharmgkbrs137852423
gwascentralrs137852423
openSNPrs137852423
23andMers137852423
23andMe allrs137852423
SNP Nexus

SNPshotrs137852423
SNPdbers137852423
MSV3drs137852423
GWAS Ctlgrs137852423
Max Magnitude0
OMIM306700
Desc
Variant0148
Relatedalso
ClinVar
Risk rs137852423(C;C)
Alt rs137852423(C;C)
Reference rs137852423(T;T)
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.154182284A>G
CLNSRC
CLNACC