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rs1057517807

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1057517807(CT;TG)
Make rs1057517807(TG;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position78304839
GenePSAT1
is asnp
is mentioned by
dbSNPrs1057517807
dbSNP (old)rs1057517807
ClinGenrs1057517807
ebirs1057517807
HLIrs1057517807
Exacrs1057517807
Gnomadrs1057517807
Varsomers1057517807
Maprs1057517807
PheGenIrs1057517807
Biobankrs1057517807
1000 genomesrs1057517807
hgdprs1057517807
ensemblrs1057517807
gopubmedrs1057517807
geneviewrs1057517807
scholarrs1057517807
googlers1057517807
pharmgkbrs1057517807
gwascentralrs1057517807
openSNPrs1057517807
23andMers1057517807
23andMe allrs1057517807
SNPshotrs1057517807
SNPdbers1057517807
MSV3drs1057517807
GWAS Ctlgrs1057517807
Max Magnitude0
ClinVar
Risk rs1057517807(TG;TG)
Alt rs1057517807(TG;TG)
Reference Rs1057517807(CT;CT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PSAT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.80919755_80919756delCTinsTG
CLNSRC
CLNACC RCV000414424.1,