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rs267606892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606892(C;C)
Make rs267606892(C;T)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position10563
GeneMT-ND3
is asnp
is mentioned by
dbSNPrs267606892
ebirs267606892
HLIrs267606892
Exacrs267606892
Varsomers267606892
Maprs267606892
PheGenIrs267606892
hapmaprs267606892
1000 genomesrs267606892
hgdprs267606892
ensemblrs267606892
gopubmedrs267606892
geneviewrs267606892
scholarrs267606892
googlers267606892
pharmgkbrs267606892
gwascentralrs267606892
openSNPrs267606892
23andMers267606892
23andMe allrs267606892
SNP Nexus

SNPshotrs267606892
SNPdbers267606892
MSV3drs267606892
GWAS Ctlgrs267606892
Max Magnitude0
ClinVar
Risk rs267606892(C;C)
Alt rs267606892(C;C)
Reference rs267606892(T;T)
Significance Pathogenic
Disease Familial colorectal cancer
Variation info
Gene ND4L
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_012920.1:m.10563T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010352.2,