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rs137852229

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852229(A;C)
Make rs137852229(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139537158
GeneF9
is asnp
is mentioned by
dbSNPrs137852229
ebirs137852229
HLIrs137852229
Exacrs137852229
Varsomers137852229
Maprs137852229
PheGenIrs137852229
hapmaprs137852229
1000 genomesrs137852229
hgdprs137852229
ensemblrs137852229
gopubmedrs137852229
geneviewrs137852229
scholarrs137852229
googlers137852229
pharmgkbrs137852229
gwascentralrs137852229
openSNPrs137852229
23andMers137852229
23andMe allrs137852229
SNP Nexus

SNPshotrs137852229
SNPdbers137852229
MSV3drs137852229
GWAS Ctlgrs137852229
Max Magnitude0
OMIM300746
Desc
Variant0017
Relatedalso
ClinVar
Risk rs137852229(C;C)
Alt rs137852229(C;C)
Reference rs137852229(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.138619317A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011320.7,