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rs61752784

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61752784(C;G)
Make rs61752784(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89330133
GenePOLG
is asnp
is mentioned by
dbSNPrs61752784
ebirs61752784
HLIrs61752784
Exacrs61752784
Varsomers61752784
Maprs61752784
PheGenIrs61752784
hapmaprs61752784
1000 genomesrs61752784
hgdprs61752784
ensemblrs61752784
gopubmedrs61752784
geneviewrs61752784
scholarrs61752784
googlers61752784
pharmgkbrs61752784
gwascentralrs61752784
openSNPrs61752784
23andMers61752784
23andMe allrs61752784
SNP Nexus

SNPshotrs61752784
SNPdbers61752784
MSV3drs61752784
GWAS Ctlgrs61752784
Max Magnitude0
ClinVar
Risk rs61752784(G;G)
Alt rs61752784(G;G)
Reference rs61752784(C;C)
Significance Other
Disease not specified Progressive sclerosing poliodystrophy
Variation info
Gene POLG
CLNDBN not specified Progressive sclerosing poliodystrophy
Reversed 0
HGVS NC_000015.9:g.89873364C>G
CLNSRC
CLNACC RCV000177165.2, RCV000233823.1,