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rs137852271

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852271(G;T)
Make rs137852271(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561805
GeneF9
is asnp
is mentioned by
dbSNPrs137852271
dbSNP (old)rs137852271
ClinGenrs137852271
ebirs137852271
HLIrs137852271
Exacrs137852271
Varsomers137852271
Maprs137852271
PheGenIrs137852271
Biobankrs137852271
1000 genomesrs137852271
hgdprs137852271
ensemblrs137852271
gopubmedrs137852271
geneviewrs137852271
scholarrs137852271
googlers137852271
pharmgkbrs137852271
gwascentralrs137852271
openSNPrs137852271
23andMers137852271
23andMe allrs137852271
SNP Nexus

SNPshotrs137852271
SNPdbers137852271
MSV3drs137852271
GWAS Ctlgrs137852271
Max Magnitude0
OMIM300746
Desc
Variant0083
Relatedalso
ClinVar
Risk rs137852271(T;T)
Alt rs137852271(T;T)
Reference Rs137852271(G;G)
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.138643964G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011385.4,