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rs121965071

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121965071(G;T)
Make rs121965071(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position186284209
GeneF11
is asnp
is mentioned by
dbSNPrs121965071
ebirs121965071
HLIrs121965071
Exacrs121965071
Varsomers121965071
Maprs121965071
PheGenIrs121965071
hapmaprs121965071
1000 genomesrs121965071
hgdprs121965071
ensemblrs121965071
gopubmedrs121965071
geneviewrs121965071
scholarrs121965071
googlers121965071
pharmgkbrs121965071
gwascentralrs121965071
openSNPrs121965071
23andMers121965071
23andMe allrs121965071
SNP Nexus

SNPshotrs121965071
SNPdbers121965071
MSV3drs121965071
GWAS Ctlgrs121965071
Max Magnitude0
OMIM264900
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121965071(A,T;A,T)
Alt rs121965071(A,T;A,T)
Reference rs121965071(G;G)
Significance Other
Disease Hereditary factor XI deficiency disease
Variation info
Gene F11
CLNDBN Hereditary factor XI deficiency disease
Reversed 0
HGVS NC_000004.11:g.187205363G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012678.26,