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rs137852251

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852251(A;G)
Make rs137852251(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561602
GeneF9
is asnp
is mentioned by
dbSNPrs137852251
ebirs137852251
HLIrs137852251
Exacrs137852251
Varsomers137852251
Maprs137852251
PheGenIrs137852251
hapmaprs137852251
1000 genomesrs137852251
hgdprs137852251
ensemblrs137852251
gopubmedrs137852251
geneviewrs137852251
scholarrs137852251
googlers137852251
pharmgkbrs137852251
gwascentralrs137852251
openSNPrs137852251
23andMers137852251
23andMe allrs137852251
SNP Nexus

SNPshotrs137852251
SNPdbers137852251
MSV3drs137852251
GWAS Ctlgrs137852251
Max Magnitude0
OMIM300746
Desc
Variant0047
Relatedalso
ClinVar
Risk rs137852251(G;G)
Alt rs137852251(G;G)
Reference rs137852251(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.138643761A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011350.5,