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rs796052919

From SNPedia

Orientationminus
Make rs796052919(-;-)
Make rs796052919(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89322773
GenePOLG
is asnp
is mentioned by
dbSNPrs796052919
ebirs796052919
HLIrs796052919
Exacrs796052919
Varsomers796052919
Maprs796052919
PheGenIrs796052919
hapmaprs796052919
1000 genomesrs796052919
hgdprs796052919
ensemblrs796052919
gopubmedrs796052919
geneviewrs796052919
scholarrs796052919
googlers796052919
pharmgkbrs796052919
gwascentralrs796052919
openSNPrs796052919
23andMers796052919
23andMe allrs796052919
SNP Nexus

SNPshotrs796052919
SNPdbers796052919
MSV3drs796052919
GWAS Ctlgrs796052919
Max Magnitude
ClinVar
Risk rs796052919(;)
Alt rs796052919(;)
Reference rs796052919(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89866004delA
CLNSRC
CLNACC RCV000188698.1,