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rs41504845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41504845(C;T)
Make rs41504845(T;T)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position15833
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs41504845
ebirs41504845
HLIrs41504845
Exacrs41504845
Varsomers41504845
Maprs41504845
PheGenIrs41504845
hapmaprs41504845
1000 genomesrs41504845
hgdprs41504845
ensemblrs41504845
gopubmedrs41504845
geneviewrs41504845
scholarrs41504845
googlers41504845
pharmgkbrs41504845
gwascentralrs41504845
openSNPrs41504845
23andMers41504845
23andMe allrs41504845
SNP Nexus

SNPshotrs41504845
SNPdbers41504845
MSV3drs41504845
GWAS Ctlgrs41504845
GMAF0.003742
Max Magnitude0

haplogroups


ClinVar
Risk rs41504845(T;T)
Alt rs41504845(T;T)
Reference rs41504845(C;C)
Significance Probable-non-pathogenic
Disease not provided
Variation info
Gene CYTB
CLNDBN not provided
Reversed 0
HGVS NC_012920.1:m.15833C>T
CLNSRC
CLNACC RCV000224196.1,