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rs121965072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121965072(C;C)
Make rs121965072(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position186288496
GeneF11, PRAMEF4
is asnp
is mentioned by
dbSNPrs121965072
ebirs121965072
HLIrs121965072
Exacrs121965072
Varsomers121965072
Maprs121965072
PheGenIrs121965072
hapmaprs121965072
1000 genomesrs121965072
hgdprs121965072
ensemblrs121965072
gopubmedrs121965072
geneviewrs121965072
scholarrs121965072
googlers121965072
pharmgkbrs121965072
gwascentralrs121965072
openSNPrs121965072
23andMers121965072
23andMe allrs121965072
SNP Nexus

SNPshotrs121965072
SNPdbers121965072
MSV3drs121965072
GWAS Ctlgrs121965072
Max Magnitude0
OMIM264900
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121965072(C;C)
Alt rs121965072(C;C)
Reference rs121965072(G;G)
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.187209650G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012679.18,