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rs137852239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852239(C;T)
Make rs137852239(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139551196
GeneF9
is asnp
is mentioned by
dbSNPrs137852239
ebirs137852239
HLIrs137852239
Exacrs137852239
Varsomers137852239
Maprs137852239
PheGenIrs137852239
hapmaprs137852239
1000 genomesrs137852239
hgdprs137852239
ensemblrs137852239
gopubmedrs137852239
geneviewrs137852239
scholarrs137852239
googlers137852239
pharmgkbrs137852239
gwascentralrs137852239
openSNPrs137852239
23andMers137852239
23andMe allrs137852239
SNP Nexus

SNPshotrs137852239
SNPdbers137852239
MSV3drs137852239
GWAS Ctlgrs137852239
Max Magnitude0
OMIM300746
Desc
Variant0029
Relatedalso
ClinVar
Risk rs137852239(T;T)
Alt rs137852239(T;T)
Reference rs137852239(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.138633355C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011335.5,