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rs137852259

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852259(A;A)
Make rs137852259(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561821
GeneF9
is asnp
is mentioned by
dbSNPrs137852259
ebirs137852259
HLIrs137852259
Exacrs137852259
Varsomers137852259
Maprs137852259
PheGenIrs137852259
hapmaprs137852259
1000 genomesrs137852259
hgdprs137852259
ensemblrs137852259
gopubmedrs137852259
geneviewrs137852259
scholarrs137852259
googlers137852259
pharmgkbrs137852259
gwascentralrs137852259
openSNPrs137852259
23andMers137852259
23andMe allrs137852259
SNP Nexus

SNPshotrs137852259
SNPdbers137852259
MSV3drs137852259
GWAS Ctlgrs137852259
Max Magnitude0
OMIM300746
Desc
Variant0056
Relatedalso
ClinVar
Risk rs137852259(A;A)
Alt rs137852259(A;A)
Reference rs137852259(G;G)
Significance Pathogenic
Disease Hereditary factor IX deficiency disease
Variation info
Gene F9
CLNDBN Hereditary factor IX deficiency disease
Reversed 0
HGVS NC_000023.10:g.138643980G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011359.7,