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rs863224170

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224170(C;C)
Make rs863224170(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position64477988
GeneMILR1, POLG2
is asnp
is mentioned by
dbSNPrs863224170
ebirs863224170
HLIrs863224170
Exacrs863224170
Varsomers863224170
Maprs863224170
PheGenIrs863224170
hapmaprs863224170
1000 genomesrs863224170
hgdprs863224170
ensemblrs863224170
gopubmedrs863224170
geneviewrs863224170
scholarrs863224170
googlers863224170
pharmgkbrs863224170
gwascentralrs863224170
openSNPrs863224170
23andMers863224170
23andMe allrs863224170
SNP Nexus

SNPshotrs863224170
SNPdbers863224170
MSV3drs863224170
GWAS Ctlgrs863224170
Max Magnitude0
ClinVar
Risk rs863224170(C;C)
Alt rs863224170(C;C)
Reference rs863224170(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MILR1 POLG2
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.62474105C>G
CLNSRC
CLNACC RCV000199111.2,