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rs202037973

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs202037973(A;G)
Make rs202037973(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89323423
GenePOLG
is asnp
is mentioned by
dbSNPrs202037973
ebirs202037973
HLIrs202037973
Exacrs202037973
Varsomers202037973
Maprs202037973
PheGenIrs202037973
hapmaprs202037973
1000 genomesrs202037973
hgdprs202037973
ensemblrs202037973
gopubmedrs202037973
geneviewrs202037973
scholarrs202037973
googlers202037973
pharmgkbrs202037973
gwascentralrs202037973
openSNPrs202037973
23andMers202037973
23andMe allrs202037973
SNP Nexus

SNPshotrs202037973
SNPdbers202037973
MSV3drs202037973
GWAS Ctlgrs202037973
Max Magnitude0
ClinVar
Risk rs202037973(G;G)
Alt rs202037973(G;G)
Reference rs202037973(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89866654A>G
CLNSRC
CLNACC RCV000188572.2,