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rs137852252

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852252(C;T)
Make rs137852252(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561683
GeneF9
is asnp
is mentioned by
dbSNPrs137852252
ebirs137852252
HLIrs137852252
Exacrs137852252
Varsomers137852252
Maprs137852252
PheGenIrs137852252
hapmaprs137852252
1000 genomesrs137852252
hgdprs137852252
ensemblrs137852252
gopubmedrs137852252
geneviewrs137852252
scholarrs137852252
googlers137852252
pharmgkbrs137852252
gwascentralrs137852252
openSNPrs137852252
23andMers137852252
23andMe allrs137852252
SNP Nexus

SNPshotrs137852252
SNPdbers137852252
MSV3drs137852252
GWAS Ctlgrs137852252
Max Magnitude0
OMIM300746
Desc
Variant0048
Relatedalso
ClinVar
Risk rs137852252(T;T)
Alt rs137852252(T;T)
Reference rs137852252(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.138643842C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011351.1,