Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224114

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224114(C;T)
Make rs863224114(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position68033224
GeneMIR4691, MIR7113, NDUFS8
is asnp
is mentioned by
dbSNPrs863224114
ebirs863224114
HLIrs863224114
Exacrs863224114
Varsomers863224114
Maprs863224114
PheGenIrs863224114
hapmaprs863224114
1000 genomesrs863224114
hgdprs863224114
ensemblrs863224114
gopubmedrs863224114
geneviewrs863224114
scholarrs863224114
googlers863224114
pharmgkbrs863224114
gwascentralrs863224114
openSNPrs863224114
23andMers863224114
23andMe allrs863224114
SNP Nexus

SNPshotrs863224114
SNPdbers863224114
MSV3drs863224114
GWAS Ctlgrs863224114
Max Magnitude0
ClinVar
Risk rs863224114(T;T)
Alt rs863224114(T;T)
Reference rs863224114(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR7113 MIR4691 NDUFS8
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67800691C>T
CLNSRC
CLNACC RCV000195877.1,