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rs1057520280

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520280(A;A)
Make rs1057520280(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position60904874
GeneERCC8
is asnp
is mentioned by
dbSNPrs1057520280
dbSNP (old)rs1057520280
ClinGenrs1057520280
ebirs1057520280
HLIrs1057520280
Exacrs1057520280
Gnomadrs1057520280
Varsomers1057520280
Maprs1057520280
PheGenIrs1057520280
Biobankrs1057520280
1000 genomesrs1057520280
hgdprs1057520280
ensemblrs1057520280
gopubmedrs1057520280
geneviewrs1057520280
scholarrs1057520280
googlers1057520280
pharmgkbrs1057520280
gwascentralrs1057520280
openSNPrs1057520280
23andMers1057520280
23andMe allrs1057520280
SNPshotrs1057520280
SNPdbers1057520280
MSV3drs1057520280
GWAS Ctlgrs1057520280
Max Magnitude0
ClinVar
Risk rs1057520280(A;A)
Alt rs1057520280(A;A)
Reference Rs1057520280(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ERCC8
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.60200701C>T
CLNSRC
CLNACC RCV000424558.1,