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rs137852266

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852266(A;A)
Make rs137852266(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561992
GeneF9
is asnp
is mentioned by
dbSNPrs137852266
ebirs137852266
HLIrs137852266
Exacrs137852266
Varsomers137852266
Maprs137852266
PheGenIrs137852266
hapmaprs137852266
1000 genomesrs137852266
hgdprs137852266
ensemblrs137852266
gopubmedrs137852266
geneviewrs137852266
scholarrs137852266
googlers137852266
pharmgkbrs137852266
gwascentralrs137852266
openSNPrs137852266
23andMers137852266
23andMe allrs137852266
SNP Nexus

SNPshotrs137852266
SNPdbers137852266
MSV3drs137852266
GWAS Ctlgrs137852266
Max Magnitude0
OMIM300746
Desc
Variant0066
Relatedalso
OMIM300746
Desc
Variant0067
Relatedalso
ClinVar
Risk rs137852266(A,T;A,T)
Alt rs137852266(A,T;A,T)
Reference rs137852266(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.138644151C>A; NC_000023.10:g.138644151C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011368.4, RCV000011369.5,