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rs28358572

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs28358572(C;C)
Make rs28358572(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position1243
is asnp
is mentioned by
dbSNPrs28358572
dbSNP (classic)rs28358572
ClinGenrs28358572
ebirs28358572
HLIrs28358572
Exacrs28358572
Gnomadrs28358572
Varsomers28358572
LitVarrs28358572
Maprs28358572
PheGenIrs28358572
Biobankrs28358572
1000 genomesrs28358572
hgdprs28358572
ensemblrs28358572
geneviewrs28358572
scholarrs28358572
googlers28358572
pharmgkbrs28358572
gwascentralrs28358572
openSNPrs28358572
23andMers28358572
SNPshotrs28358572
SNPdbers28358572
MSV3drs28358572
GWAS Ctlgrs28358572
GMAF0.01123
Max Magnitude0
? (C;C) (C;T) (T;T) 28



[PMID 11245424] Detection of mitochondrial DNA mutations in pancreatic cancer offers a "mass"-ive advantage over detection of nuclear DNA mutations.


ClinVar
Risk rs28358572(C;C)
Alt rs28358572(C;C)
Reference Rs28358572(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene
CLNDBN not specified
Reversed 0
HGVS NC_012920.1:m.1243T>C
CLNSRC
CLNACC RCV000035037.2,