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rs137852265

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852265(A;A)
Make rs137852265(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561925
GeneF9
is asnp
is mentioned by
dbSNPrs137852265
ebirs137852265
HLIrs137852265
Exacrs137852265
Varsomers137852265
Maprs137852265
PheGenIrs137852265
hapmaprs137852265
1000 genomesrs137852265
hgdprs137852265
ensemblrs137852265
gopubmedrs137852265
geneviewrs137852265
scholarrs137852265
googlers137852265
pharmgkbrs137852265
gwascentralrs137852265
openSNPrs137852265
23andMers137852265
23andMe allrs137852265
SNP Nexus

SNPshotrs137852265
SNPdbers137852265
MSV3drs137852265
GWAS Ctlgrs137852265
Max Magnitude0
OMIM300746
Desc
Variant0064
Relatedalso
ClinVar
Risk rs137852265(A,T;A,T)
Alt rs137852265(A,T;A,T)
Reference rs137852265(C;C)
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.138644084C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011366.7,