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rs137852245

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852245(A;T)
Make rs137852245(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139551251
GeneF9
is asnp
is mentioned by
dbSNPrs137852245
ebirs137852245
HLIrs137852245
Exacrs137852245
Varsomers137852245
Maprs137852245
PheGenIrs137852245
hapmaprs137852245
1000 genomesrs137852245
hgdprs137852245
ensemblrs137852245
gopubmedrs137852245
geneviewrs137852245
scholarrs137852245
googlers137852245
pharmgkbrs137852245
gwascentralrs137852245
openSNPrs137852245
23andMers137852245
23andMe allrs137852245
SNP Nexus

SNPshotrs137852245
SNPdbers137852245
MSV3drs137852245
GWAS Ctlgrs137852245
Max Magnitude0
OMIM300746
Desc
Variant0036
Relatedalso
ClinVar
Risk rs137852245(T;T)
Alt rs137852245(T;T)
Reference rs137852245(A;A)
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.138633410A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011342.1,