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rs137852270

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852270(A;T)
Make rs137852270(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139562054
GeneF9
is asnp
is mentioned by
dbSNPrs137852270
ebirs137852270
HLIrs137852270
Exacrs137852270
Varsomers137852270
Maprs137852270
PheGenIrs137852270
hapmaprs137852270
1000 genomesrs137852270
hgdprs137852270
ensemblrs137852270
gopubmedrs137852270
geneviewrs137852270
scholarrs137852270
googlers137852270
pharmgkbrs137852270
gwascentralrs137852270
openSNPrs137852270
23andMers137852270
23andMe allrs137852270
SNP Nexus

SNPshotrs137852270
SNPdbers137852270
MSV3drs137852270
GWAS Ctlgrs137852270
Max Magnitude0
OMIM300746
Desc
Variant0071
Relatedalso
ClinVar
Risk rs137852270(T;T)
Alt rs137852270(T;T)
Reference rs137852270(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.138644213A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011373.2,