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rs869312882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs869312882(-;C)
Make rs869312882(C;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position14248
GeneND6
is asnp
is mentioned by
dbSNPrs869312882
dbSNP (old)rs869312882
ClinGenrs869312882
ebirs869312882
HLIrs869312882
Exacrs869312882
Varsomers869312882
Maprs869312882
PheGenIrs869312882
Biobankrs869312882
1000 genomesrs869312882
hgdprs869312882
ensemblrs869312882
gopubmedrs869312882
geneviewrs869312882
scholarrs869312882
googlers869312882
pharmgkbrs869312882
gwascentralrs869312882
openSNPrs869312882
23andMers869312882
23andMe allrs869312882
SNP Nexus

SNPshotrs869312882
SNPdbers869312882
MSV3drs869312882
GWAS Ctlgrs869312882
Max Magnitude0
ClinVar
Risk rs869312882(C;C)
Alt rs869312882(C;C)
Reference Rs869312882(-;-)
Significance Pathogenic
Disease Oxyphilic adenoma
Variation info
Gene ND6
CLNDBN Oxyphilic adenoma
Reversed 0
HGVS NC_012920.1:m.14248dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000210344.1,