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rs113994100

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs113994100(G;G)
Make rs113994100(G;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position89317531
GeneFANCI, POLG
is asnp
is mentioned by
dbSNPrs113994100
ebirs113994100
HLIrs113994100
Exacrs113994100
Varsomers113994100
Maprs113994100
PheGenIrs113994100
hapmaprs113994100
1000 genomesrs113994100
hgdprs113994100
ensemblrs113994100
gopubmedrs113994100
geneviewrs113994100
scholarrs113994100
googlers113994100
pharmgkbrs113994100
gwascentralrs113994100
openSNPrs113994100
23andMers113994100
23andMe allrs113994100
SNP Nexus

SNPshotrs113994100
SNPdbers113994100
MSV3drs113994100
GWAS Ctlgrs113994100
Max Magnitude0
ClinVar
Risk rs113994100(C,G;C,G)
Alt rs113994100(C,G;C,G)
Reference rs113994100(T;T)
Significance Pathogenic
Disease Mitochondrial diseases not provided
Variation info
Gene POLG FANCI
CLNDBN Mitochondrial diseases not provided
Reversed 1
HGVS NC_000015.9:g.89860762A>C; NC_000015.9:g.89860762A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020478.1, RCV000188682.1,