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rs199759055

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199759055(A;A)
Make rs199759055(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89328699
GeneMIR6766, POLG
is asnp
is mentioned by
dbSNPrs199759055
ebirs199759055
HLIrs199759055
Exacrs199759055
Varsomers199759055
Maprs199759055
PheGenIrs199759055
hapmaprs199759055
1000 genomesrs199759055
hgdprs199759055
ensemblrs199759055
gopubmedrs199759055
geneviewrs199759055
scholarrs199759055
googlers199759055
pharmgkbrs199759055
gwascentralrs199759055
openSNPrs199759055
23andMers199759055
23andMe allrs199759055
SNP Nexus

SNPshotrs199759055
SNPdbers199759055
MSV3drs199759055
GWAS Ctlgrs199759055
Max Magnitude0
ClinVar
Risk rs199759055(A;A)
Alt rs199759055(A;A)
Reference rs199759055(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR6766 POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89871930G>A
CLNSRC
CLNACC RCV000188650.2,