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rs137852242

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852242(G;T)
Make rs137852242(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139551220
GeneF9
is asnp
is mentioned by
dbSNPrs137852242
ebirs137852242
HLIrs137852242
Exacrs137852242
Varsomers137852242
Maprs137852242
PheGenIrs137852242
hapmaprs137852242
1000 genomesrs137852242
hgdprs137852242
ensemblrs137852242
gopubmedrs137852242
geneviewrs137852242
scholarrs137852242
googlers137852242
pharmgkbrs137852242
gwascentralrs137852242
openSNPrs137852242
23andMers137852242
23andMe allrs137852242
SNP Nexus

SNPshotrs137852242
SNPdbers137852242
MSV3drs137852242
GWAS Ctlgrs137852242
Max Magnitude0
OMIM300746
Desc
Variant0032
Relatedalso
ClinVar
Risk rs137852242(T;T)
Alt rs137852242(T;T)
Reference rs137852242(G;G)
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.138633379G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011338.6,