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rs137852258

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852258(C;T)
Make rs137852258(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561820
GeneF9
is asnp
is mentioned by
dbSNPrs137852258
ebirs137852258
HLIrs137852258
Exacrs137852258
Varsomers137852258
Maprs137852258
PheGenIrs137852258
hapmaprs137852258
1000 genomesrs137852258
hgdprs137852258
ensemblrs137852258
gopubmedrs137852258
geneviewrs137852258
scholarrs137852258
googlers137852258
pharmgkbrs137852258
gwascentralrs137852258
openSNPrs137852258
23andMers137852258
23andMe allrs137852258
SNP Nexus

SNPshotrs137852258
SNPdbers137852258
MSV3drs137852258
GWAS Ctlgrs137852258
Max Magnitude0
OMIM300746
Desc
Variant0055
Relatedalso
ClinVar
Risk rs137852258(T;T)
Alt rs137852258(T;T)
Reference rs137852258(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.138643979C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011358.2,