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rs137852223

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852223(C;T)
Make rs137852223(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139537090
GeneF9
is asnp
is mentioned by
dbSNPrs137852223
ebirs137852223
HLIrs137852223
Exacrs137852223
Varsomers137852223
Maprs137852223
PheGenIrs137852223
hapmaprs137852223
1000 genomesrs137852223
hgdprs137852223
ensemblrs137852223
gopubmedrs137852223
geneviewrs137852223
scholarrs137852223
googlers137852223
pharmgkbrs137852223
gwascentralrs137852223
openSNPrs137852223
23andMers137852223
23andMe allrs137852223
SNP Nexus

SNPshotrs137852223
SNPdbers137852223
MSV3drs137852223
GWAS Ctlgrs137852223
Max Magnitude0
OMIM300746
Desc
Variant0011
Relatedalso
ClinVar
Risk rs137852223(T;T)
Alt rs137852223(T;T)
Reference rs137852223(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.138619249C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011313.4,