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rs1060499749

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499749(C;T)
Make rs1060499749(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position42352288
GenePTPRT
is asnp
is mentioned by
dbSNPrs1060499749
dbSNP (old)rs1060499749
ClinGenrs1060499749
ebirs1060499749
HLIrs1060499749
Exacrs1060499749
Gnomadrs1060499749
Varsomers1060499749
Maprs1060499749
PheGenIrs1060499749
Biobankrs1060499749
1000 genomesrs1060499749
hgdprs1060499749
ensemblrs1060499749
gopubmedrs1060499749
geneviewrs1060499749
scholarrs1060499749
googlers1060499749
pharmgkbrs1060499749
gwascentralrs1060499749
openSNPrs1060499749
23andMers1060499749
23andMe allrs1060499749
SNPshotrs1060499749
SNPdbers1060499749
MSV3drs1060499749
GWAS Ctlgrs1060499749
Max Magnitude0
ClinVar
Risk rs1060499749(T;T)
Alt rs1060499749(T;T)
Reference Rs1060499749(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene PTPRT
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000020.10:g.40980928G>A
CLNSRC
CLNACC RCV000454175.1,