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rs138929605

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs138929605(A;A)
Make rs138929605(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89330106
GenePOLG
is asnp
is mentioned by
dbSNPrs138929605
ebirs138929605
HLIrs138929605
Exacrs138929605
Varsomers138929605
Maprs138929605
PheGenIrs138929605
hapmaprs138929605
1000 genomesrs138929605
hgdprs138929605
ensemblrs138929605
gopubmedrs138929605
geneviewrs138929605
scholarrs138929605
googlers138929605
pharmgkbrs138929605
gwascentralrs138929605
openSNPrs138929605
23andMers138929605
23andMe allrs138929605
SNP Nexus

SNPshotrs138929605
SNPdbers138929605
MSV3drs138929605
GWAS Ctlgrs138929605
Max Magnitude0
ClinVar
Risk rs138929605(A,C;A,C)
Alt rs138929605(A,C;A,C)
Reference rs138929605(T;T)
Significance Pathogenic
Disease not provided Progressive sclerosing poliodystrophy
Variation info
Gene POLG
CLNDBN not provided Progressive sclerosing poliodystrophy
Reversed 0
HGVS NC_000015.9:g.89873337T>A
CLNSRC
CLNACC RCV000188643.2, RCV000231645.1,