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rs137852227

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852227(C;T)
Make rs137852227(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139537144
GeneF9
is asnp
is mentioned by
dbSNPrs137852227
ebirs137852227
HLIrs137852227
Exacrs137852227
Varsomers137852227
Maprs137852227
PheGenIrs137852227
hapmaprs137852227
1000 genomesrs137852227
hgdprs137852227
ensemblrs137852227
gopubmedrs137852227
geneviewrs137852227
scholarrs137852227
googlers137852227
pharmgkbrs137852227
gwascentralrs137852227
openSNPrs137852227
23andMers137852227
23andMe allrs137852227
SNP Nexus

SNPshotrs137852227
SNPdbers137852227
MSV3drs137852227
GWAS Ctlgrs137852227
Max Magnitude0
OMIM300746
Desc
Variant0015
Relatedalso
ClinVar
Risk rs137852227(T;T)
Alt rs137852227(T;T)
Reference rs137852227(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.138619303C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011318.3,