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rs771623994

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771623994(C;T)
Make rs771623994(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position89327166
GeneMIR6766, POLG
is asnp
is mentioned by
dbSNPrs771623994
dbSNP (classic)rs771623994
ClinGenrs771623994
ebirs771623994
HLIrs771623994
Exacrs771623994
Gnomadrs771623994
Varsomers771623994
LitVarrs771623994
Maprs771623994
PheGenIrs771623994
Biobankrs771623994
1000 genomesrs771623994
hgdprs771623994
ensemblrs771623994
geneviewrs771623994
scholarrs771623994
googlers771623994
pharmgkbrs771623994
gwascentralrs771623994
openSNPrs771623994
23andMers771623994
SNPshotrs771623994
SNPdbers771623994
MSV3drs771623994
GWAS Ctlgrs771623994
Max Magnitude0
ClinVar
Risk rs771623994(T;T)
Alt rs771623994(T;T)
Reference Rs771623994(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR6766 POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89870397C>T
CLNSRC
CLNACC RCV000359026.2,