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rs137852414

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852414(A;A)
Make rs137852414(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154961120
GeneF8
is asnp
is mentioned by
dbSNPrs137852414
ebirs137852414
HLIrs137852414
Exacrs137852414
Varsomers137852414
Maprs137852414
PheGenIrs137852414
hapmaprs137852414
1000 genomesrs137852414
hgdprs137852414
ensemblrs137852414
gopubmedrs137852414
geneviewrs137852414
scholarrs137852414
googlers137852414
pharmgkbrs137852414
gwascentralrs137852414
openSNPrs137852414
23andMers137852414
23andMe allrs137852414
SNP Nexus

SNPshotrs137852414
SNPdbers137852414
MSV3drs137852414
GWAS Ctlgrs137852414
Merged fromRs28936969
Max Magnitude0
OMIM306700
Desc
Variant0134
Relatedalso
ClinVar
Risk rs137852414(A;A)
Alt rs137852414(A;A)
Reference rs137852414(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.154189395C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010930.7,