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rs207459996

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs207459996(C;C)
Make rs207459996(C;T)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position15572
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs207459996
ebirs207459996
HLIrs207459996
Exacrs207459996
Varsomers207459996
Maprs207459996
PheGenIrs207459996
hapmaprs207459996
1000 genomesrs207459996
hgdprs207459996
ensemblrs207459996
gopubmedrs207459996
geneviewrs207459996
scholarrs207459996
googlers207459996
pharmgkbrs207459996
gwascentralrs207459996
openSNPrs207459996
23andMers207459996
23andMe allrs207459996
SNP Nexus

SNPshotrs207459996
SNPdbers207459996
MSV3drs207459996
GWAS Ctlgrs207459996
Max Magnitude0
ClinVar
Risk rs207459996(C;C)
Alt rs207459996(C;C)
Reference rs207459996(T;T)
Significance Pathogenic
Disease Familial colorectal cancer
Variation info
Gene CYTB
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_012920.1:m.15572T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010315.4,