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rs137852237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852237(C;T)
Make rs137852237(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139551112
GeneF9
is asnp
is mentioned by
dbSNPrs137852237
ebirs137852237
HLIrs137852237
Exacrs137852237
Varsomers137852237
Maprs137852237
PheGenIrs137852237
hapmaprs137852237
1000 genomesrs137852237
hgdprs137852237
ensemblrs137852237
gopubmedrs137852237
geneviewrs137852237
scholarrs137852237
googlers137852237
pharmgkbrs137852237
gwascentralrs137852237
openSNPrs137852237
23andMers137852237
23andMe allrs137852237
SNP Nexus

SNPshotrs137852237
SNPdbers137852237
MSV3drs137852237
GWAS Ctlgrs137852237
Max Magnitude0
OMIM300746
Desc
Variant0026
Relatedalso
ClinVar
Risk rs137852237(T;T)
Alt rs137852237(T;T)
Reference rs137852237(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.138633271C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011330.5,