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rs137852411

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852411(C;C)
Make rs137852411(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154961138
GeneF8
is asnp
is mentioned by
dbSNPrs137852411
ebirs137852411
HLIrs137852411
Exacrs137852411
Varsomers137852411
Maprs137852411
PheGenIrs137852411
hapmaprs137852411
1000 genomesrs137852411
hgdprs137852411
ensemblrs137852411
gopubmedrs137852411
geneviewrs137852411
scholarrs137852411
googlers137852411
pharmgkbrs137852411
gwascentralrs137852411
openSNPrs137852411
23andMers137852411
23andMe allrs137852411
SNP Nexus

SNPshotrs137852411
SNPdbers137852411
MSV3drs137852411
GWAS Ctlgrs137852411
Merged fromRs28937274
Max Magnitude0
OMIM306700
Desc
Variant0131
Relatedalso
ClinVar
Risk rs137852411(C;C)
Alt rs137852411(C;C)
Reference rs137852411(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.154189413A>G
CLNSRC
CLNACC