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rs139562274

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139562274(A;A)
Make rs139562274(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89317389
GeneFANCI, POLG
is asnp
is mentioned by
dbSNPrs139562274
ebirs139562274
HLIrs139562274
Exacrs139562274
Varsomers139562274
Maprs139562274
PheGenIrs139562274
hapmaprs139562274
1000 genomesrs139562274
hgdprs139562274
ensemblrs139562274
gopubmedrs139562274
geneviewrs139562274
scholarrs139562274
googlers139562274
pharmgkbrs139562274
gwascentralrs139562274
openSNPrs139562274
23andMers139562274
23andMe allrs139562274
SNP Nexus

SNPshotrs139562274
SNPdbers139562274
MSV3drs139562274
GWAS Ctlgrs139562274
Max Magnitude0
ClinVar
Risk rs139562274(A,C;A,C)
Alt rs139562274(A,C;A,C)
Reference rs139562274(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG FANCI
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89860620G>C
CLNSRC
CLNACC RCV000188630.1,