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rs1800455

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1800455(C;C)
Make rs1800455(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139560836
GeneF9
is asnp
is mentioned by
dbSNPrs1800455
ebirs1800455
HLIrs1800455
Exacrs1800455
Varsomers1800455
Maprs1800455
PheGenIrs1800455
hapmaprs1800455
1000 genomesrs1800455
hgdprs1800455
ensemblrs1800455
gopubmedrs1800455
geneviewrs1800455
scholarrs1800455
googlers1800455
pharmgkbrs1800455
gwascentralrs1800455
openSNPrs1800455
23andMers1800455
23andMe allrs1800455
SNP Nexus

SNPshotrs1800455
SNPdbers1800455
MSV3drs1800455
GWAS Ctlgrs1800455
GMAF0.001814
Max Magnitude0
OMIM300746
Desc
Variant0041
Relatedalso
ClinVar
Risk rs1800455(C;C)
Alt rs1800455(C;C)
Reference rs1800455(T;T)
Significance Non-pathogenic
Disease FACTOR IX
Variation info
Gene F9
CLNDBN FACTOR IX, DNA POLYMORPHISM
Reversed 0
HGVS NC_000023.10:g.138642995T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011346.2,