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rs207459995

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs207459995(A;A)
Make rs207459995(A;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position14985
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs207459995
ClinGenrs207459995
ebirs207459995
HLIrs207459995
Exacrs207459995
Varsomers207459995
Maprs207459995
PheGenIrs207459995
hapmaprs207459995
1000 genomesrs207459995
hgdprs207459995
ensemblrs207459995
gopubmedrs207459995
geneviewrs207459995
scholarrs207459995
googlers207459995
pharmgkbrs207459995
gwascentralrs207459995
openSNPrs207459995
23andMers207459995
23andMe allrs207459995
SNP Nexus

SNPshotrs207459995
SNPdbers207459995
MSV3drs207459995
GWAS Ctlgrs207459995
Max Magnitude0
ClinVar
Risk rs207459995(A;A)
Alt rs207459995(A;A)
Reference Rs207459995(G;G)
Significance Pathogenic
Disease Familial colorectal cancer
Variation info
Gene CYTB
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_012920.1:m.14985G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010314.2,