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rs121965066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121965066(A;A)
Make rs121965066(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position186274228
GeneF11
is asnp
is mentioned by
dbSNPrs121965066
ebirs121965066
HLIrs121965066
Exacrs121965066
Varsomers121965066
Maprs121965066
PheGenIrs121965066
hapmaprs121965066
1000 genomesrs121965066
hgdprs121965066
ensemblrs121965066
gopubmedrs121965066
geneviewrs121965066
scholarrs121965066
googlers121965066
pharmgkbrs121965066
gwascentralrs121965066
openSNPrs121965066
23andMers121965066
23andMe allrs121965066
SNP Nexus

SNPshotrs121965066
SNPdbers121965066
MSV3drs121965066
GWAS Ctlgrs121965066
Max Magnitude0
OMIM264900
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121965066(A;A)
Alt rs121965066(A;A)
Reference rs121965066(C;C)
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.187195382C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012671.25,