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rs1057518035

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518035(A;G)
Make rs1057518035(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position89317538
GeneFANCI, POLG
is asnp
is mentioned by
dbSNPrs1057518035
dbSNP (old)rs1057518035
ClinGenrs1057518035
ebirs1057518035
HLIrs1057518035
Exacrs1057518035
Gnomadrs1057518035
Varsomers1057518035
Maprs1057518035
PheGenIrs1057518035
Biobankrs1057518035
1000 genomesrs1057518035
hgdprs1057518035
ensemblrs1057518035
gopubmedrs1057518035
geneviewrs1057518035
scholarrs1057518035
googlers1057518035
pharmgkbrs1057518035
gwascentralrs1057518035
openSNPrs1057518035
23andMers1057518035
23andMe allrs1057518035
SNPshotrs1057518035
SNPdbers1057518035
MSV3drs1057518035
GWAS Ctlgrs1057518035
Max Magnitude0
ClinVar
Risk rs1057518035(G;G)
Alt rs1057518035(G;G)
Reference Rs1057518035(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG FANCI
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89860769T>C
CLNSRC
CLNACC RCV000414416.1,