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rs775538075

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs775538075(A;G)
Make rs775538075(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89327300
GeneMIR6766, POLG
is asnp
is mentioned by
dbSNPrs775538075
ebirs775538075
HLIrs775538075
Exacrs775538075
Varsomers775538075
Maprs775538075
PheGenIrs775538075
hapmaprs775538075
1000 genomesrs775538075
hgdprs775538075
ensemblrs775538075
gopubmedrs775538075
geneviewrs775538075
scholarrs775538075
googlers775538075
pharmgkbrs775538075
gwascentralrs775538075
openSNPrs775538075
23andMers775538075
23andMe allrs775538075
SNP Nexus

SNPshotrs775538075
SNPdbers775538075
MSV3drs775538075
GWAS Ctlgrs775538075
Max Magnitude0
ClinVar
Risk rs775538075(G;G)
Alt rs775538075(G;G)
Reference rs775538075(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR6766 POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89870531A>G
CLNSRC
CLNACC RCV000188654.1,