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rs137852272

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852272(C;T)
Make rs137852272(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139548455
GeneF9
is asnp
is mentioned by
dbSNPrs137852272
ebirs137852272
HLIrs137852272
Exacrs137852272
Varsomers137852272
Maprs137852272
PheGenIrs137852272
hapmaprs137852272
1000 genomesrs137852272
hgdprs137852272
ensemblrs137852272
gopubmedrs137852272
geneviewrs137852272
scholarrs137852272
googlers137852272
pharmgkbrs137852272
gwascentralrs137852272
openSNPrs137852272
23andMers137852272
23andMe allrs137852272
SNP Nexus

SNPshotrs137852272
SNPdbers137852272
MSV3drs137852272
GWAS Ctlgrs137852272
Max Magnitude0
OMIM300746
Desc
Variant0084
Relatedalso
ClinVar
Risk rs137852272(T;T)
Alt rs137852272(T;T)
Reference rs137852272(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.138630614C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011386.4,