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rs796052916

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052916(A;G)
Make rs796052916(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89328795
GeneMIR6766, POLG
is asnp
is mentioned by
dbSNPrs796052916
ebirs796052916
HLIrs796052916
Exacrs796052916
Varsomers796052916
Maprs796052916
PheGenIrs796052916
hapmaprs796052916
1000 genomesrs796052916
hgdprs796052916
ensemblrs796052916
gopubmedrs796052916
geneviewrs796052916
scholarrs796052916
googlers796052916
pharmgkbrs796052916
gwascentralrs796052916
openSNPrs796052916
23andMers796052916
23andMe allrs796052916
SNP Nexus

SNPshotrs796052916
SNPdbers796052916
MSV3drs796052916
GWAS Ctlgrs796052916
Max Magnitude0
ClinVar
Risk rs796052916(G;G)
Alt rs796052916(G;G)
Reference rs796052916(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR6766 POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89872026T>C
CLNSRC
CLNACC RCV000188692.2,