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rs137852241

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852241(A;A)
Make rs137852241(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139551218
GeneF9
is asnp
is mentioned by
dbSNPrs137852241
ebirs137852241
HLIrs137852241
Exacrs137852241
Varsomers137852241
Maprs137852241
PheGenIrs137852241
hapmaprs137852241
1000 genomesrs137852241
hgdprs137852241
ensemblrs137852241
gopubmedrs137852241
geneviewrs137852241
scholarrs137852241
googlers137852241
pharmgkbrs137852241
gwascentralrs137852241
openSNPrs137852241
23andMers137852241
23andMe allrs137852241
SNP Nexus

SNPshotrs137852241
SNPdbers137852241
MSV3drs137852241
GWAS Ctlgrs137852241
Max Magnitude0
OMIM300746
Desc
Variant0031
Relatedalso
ClinVar
Risk rs137852241(A;A)
Alt rs137852241(A;A)
Reference rs137852241(G;G)
Significance Pathogenic
Disease Hemophilia b(m)
Variation info
Gene F9
CLNDBN Hemophilia b(m)
Reversed 0
HGVS NC_000023.10:g.138633377G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011337.7,