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rs121965067

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121965067(A;A)
Make rs121965067(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position186284167
GeneF11
is asnp
is mentioned by
dbSNPrs121965067
ebirs121965067
HLIrs121965067
Exacrs121965067
Varsomers121965067
Maprs121965067
PheGenIrs121965067
hapmaprs121965067
1000 genomesrs121965067
hgdprs121965067
ensemblrs121965067
gopubmedrs121965067
geneviewrs121965067
scholarrs121965067
googlers121965067
pharmgkbrs121965067
gwascentralrs121965067
openSNPrs121965067
23andMers121965067
23andMe allrs121965067
SNP Nexus

SNPshotrs121965067
SNPdbers121965067
MSV3drs121965067
GWAS Ctlgrs121965067
Max Magnitude0
OMIM264900
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121965067(A;A)
Alt rs121965067(A;A)
Reference rs121965067(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.187205321C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012672.24,