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rs137852282

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852282(C;C)
Make rs137852282(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561854
GeneF9
is asnp
is mentioned by
dbSNPrs137852282
ebirs137852282
HLIrs137852282
Exacrs137852282
Varsomers137852282
Maprs137852282
PheGenIrs137852282
hapmaprs137852282
1000 genomesrs137852282
hgdprs137852282
ensemblrs137852282
gopubmedrs137852282
geneviewrs137852282
scholarrs137852282
googlers137852282
pharmgkbrs137852282
gwascentralrs137852282
openSNPrs137852282
23andMers137852282
23andMe allrs137852282
SNP Nexus

SNPshotrs137852282
SNPdbers137852282
MSV3drs137852282
GWAS Ctlgrs137852282
Max Magnitude0
OMIM300746
Desc
Variant0108
Relatedalso
ClinVar
Risk rs137852282(C;C)
Alt rs137852282(C;C)
Reference rs137852282(T;T)
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.138644013T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011410.4,