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rs121965065

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121965065(G;G)
Make rs121965065(G;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position186285711
GeneF11, PRAMEF4
is asnp
is mentioned by
dbSNPrs121965065
ebirs121965065
HLIrs121965065
Exacrs121965065
Varsomers121965065
Maprs121965065
PheGenIrs121965065
hapmaprs121965065
1000 genomesrs121965065
hgdprs121965065
ensemblrs121965065
gopubmedrs121965065
geneviewrs121965065
scholarrs121965065
googlers121965065
pharmgkbrs121965065
gwascentralrs121965065
openSNPrs121965065
23andMers121965065
23andMe allrs121965065
SNP Nexus

SNPshotrs121965065
SNPdbers121965065
MSV3drs121965065
GWAS Ctlgrs121965065
Max Magnitude0
OMIM264900
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121965065(G;G)
Alt rs121965065(G;G)
Reference rs121965065(T;T)
Significance Pathogenic
Disease Hereditary factor XI deficiency disease
Variation info
Gene F11-AS1 F11
CLNDBN Hereditary factor XI deficiency disease
Reversed 0
HGVS NC_000004.11:g.187206865T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012670.21,