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rs137852280

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852280(A;A)
Make rs137852280(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561941
GeneF9
is asnp
is mentioned by
dbSNPrs137852280
ebirs137852280
HLIrs137852280
Exacrs137852280
Varsomers137852280
Maprs137852280
PheGenIrs137852280
hapmaprs137852280
1000 genomesrs137852280
hgdprs137852280
ensemblrs137852280
gopubmedrs137852280
geneviewrs137852280
scholarrs137852280
googlers137852280
pharmgkbrs137852280
gwascentralrs137852280
openSNPrs137852280
23andMers137852280
23andMe allrs137852280
SNP Nexus

SNPshotrs137852280
SNPdbers137852280
MSV3drs137852280
GWAS Ctlgrs137852280
Max Magnitude0
OMIM300746
Desc
Variant0101
Relatedalso
ClinVar
Risk rs137852280(A;A)
Alt rs137852280(A;A)
Reference rs137852280(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.138644100T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011403.4,