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rs1801202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1801202(C;T)
Make rs1801202(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561592
GeneF9
is asnp
is mentioned by
dbSNPrs1801202
ebirs1801202
HLIrs1801202
Exacrs1801202
Varsomers1801202
Maprs1801202
PheGenIrs1801202
hapmaprs1801202
1000 genomesrs1801202
hgdprs1801202
ensemblrs1801202
gopubmedrs1801202
geneviewrs1801202
scholarrs1801202
googlers1801202
pharmgkbrs1801202
gwascentralrs1801202
openSNPrs1801202
23andMers1801202
23andMe allrs1801202
SNP Nexus

SNPshotrs1801202
SNPdbers1801202
MSV3drs1801202
GWAS Ctlgrs1801202
Max Magnitude0
OMIM300746
Desc
Variant0085
Relatedalso
ClinVar
Risk rs1801202(T;T)
Alt rs1801202(T;T)
Reference rs1801202(C;C)
Significance Non-pathogenic
Disease FACTOR IX POLYMORPHISM
Variation info
Gene F9
CLNDBN FACTOR IX POLYMORPHISM
Reversed 0
HGVS NC_000023.10:g.138643751C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011387.1,