Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057517935

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs1057517935(AA;AA)
Make rs1057517935(AA;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position112450360
GenePTPN11
is asnp
is mentioned by
dbSNPrs1057517935
dbSNP (old)rs1057517935
ClinGenrs1057517935
ebirs1057517935
HLIrs1057517935
Exacrs1057517935
Gnomadrs1057517935
Varsomers1057517935
Maprs1057517935
PheGenIrs1057517935
Biobankrs1057517935
1000 genomesrs1057517935
hgdprs1057517935
ensemblrs1057517935
gopubmedrs1057517935
geneviewrs1057517935
scholarrs1057517935
googlers1057517935
pharmgkbrs1057517935
gwascentralrs1057517935
openSNPrs1057517935
23andMers1057517935
23andMe allrs1057517935
SNPshotrs1057517935
SNPdbers1057517935
MSV3drs1057517935
GWAS Ctlgrs1057517935
Max Magnitude0
ClinVar
Risk rs1057517935(AA;AA)
Alt rs1057517935(AA;AA)
Reference Rs1057517935(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene PTPN11
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.112888164_112888165delTGinsAA
CLNSRC
CLNACC RCV000412983.1,