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rs121965069

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121965069(C;C)
Make rs121965069(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position186271719
GeneF11
is asnp
is mentioned by
dbSNPrs121965069
ebirs121965069
HLIrs121965069
Exacrs121965069
Varsomers121965069
Maprs121965069
PheGenIrs121965069
hapmaprs121965069
1000 genomesrs121965069
hgdprs121965069
ensemblrs121965069
gopubmedrs121965069
geneviewrs121965069
scholarrs121965069
googlers121965069
pharmgkbrs121965069
gwascentralrs121965069
openSNPrs121965069
23andMers121965069
23andMe allrs121965069
SNP Nexus

SNPshotrs121965069
SNPdbers121965069
MSV3drs121965069
GWAS Ctlgrs121965069
Max Magnitude0
OMIM264900
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121965069(C;C)
Alt rs121965069(C;C)
Reference rs121965069(T;T)
Significance Pathogenic
Disease Hereditary factor XI deficiency disease
Variation info
Gene F11
CLNDBN Hereditary factor XI deficiency disease
Reversed 0
HGVS NC_000004.11:g.187192873T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012676.14,