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rs1057517810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517810(A;G)
Make rs1057517810(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position112230677
GenePTS
is asnp
is mentioned by
dbSNPrs1057517810
dbSNP (old)rs1057517810
ClinGenrs1057517810
ebirs1057517810
HLIrs1057517810
Exacrs1057517810
Gnomadrs1057517810
Varsomers1057517810
Maprs1057517810
PheGenIrs1057517810
Biobankrs1057517810
1000 genomesrs1057517810
hgdprs1057517810
ensemblrs1057517810
gopubmedrs1057517810
geneviewrs1057517810
scholarrs1057517810
googlers1057517810
pharmgkbrs1057517810
gwascentralrs1057517810
openSNPrs1057517810
23andMers1057517810
23andMe allrs1057517810
SNPshotrs1057517810
SNPdbers1057517810
MSV3drs1057517810
GWAS Ctlgrs1057517810
Max Magnitude0
ClinVar
Risk rs1057517810(G;G)
Alt rs1057517810(G;G)
Reference Rs1057517810(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTS
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.112101400A>G
CLNSRC
CLNACC RCV000413378.1,