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rs774610098

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs774610098(A;G)
Make rs774610098(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89327317
GeneMIR6766, POLG
is asnp
is mentioned by
dbSNPrs774610098
ebirs774610098
HLIrs774610098
Exacrs774610098
Varsomers774610098
Maprs774610098
PheGenIrs774610098
hapmaprs774610098
1000 genomesrs774610098
hgdprs774610098
ensemblrs774610098
gopubmedrs774610098
geneviewrs774610098
scholarrs774610098
googlers774610098
pharmgkbrs774610098
gwascentralrs774610098
openSNPrs774610098
23andMers774610098
23andMe allrs774610098
SNP Nexus

SNPshotrs774610098
SNPdbers774610098
MSV3drs774610098
GWAS Ctlgrs774610098
Max Magnitude0
ClinVar
Risk rs774610098(G;G)
Alt rs774610098(G;G)
Reference rs774610098(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR6766 POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89870548A>G
CLNSRC
CLNACC RCV000188653.1,