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rs121965068

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121965068(C;T)
Make rs121965068(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position186284245
GeneF11
is asnp
is mentioned by
dbSNPrs121965068
ebirs121965068
HLIrs121965068
Exacrs121965068
Varsomers121965068
Maprs121965068
PheGenIrs121965068
hapmaprs121965068
1000 genomesrs121965068
hgdprs121965068
ensemblrs121965068
gopubmedrs121965068
geneviewrs121965068
scholarrs121965068
googlers121965068
pharmgkbrs121965068
gwascentralrs121965068
openSNPrs121965068
23andMers121965068
23andMe allrs121965068
SNP Nexus

SNPshotrs121965068
SNPdbers121965068
MSV3drs121965068
GWAS Ctlgrs121965068
Merged fromRs28934901
Max Magnitude0
OMIM264900
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121965068(T;T)
Alt rs121965068(T;T)
Reference rs121965068(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.187205399C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012674.24,