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

rs1064797097

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome17
Position60656797
GenePPM1D
is asnp
is mentioned by
dbSNPrs1064797097
dbSNP (old)rs1064797097
ClinGenrs1064797097
ebirs1064797097
HLIrs1064797097
Exacrs1064797097
Gnomadrs1064797097
Varsomers1064797097
Maprs1064797097
PheGenIrs1064797097
Biobankrs1064797097
1000 genomesrs1064797097
hgdprs1064797097
ensemblrs1064797097
gopubmedrs1064797097
geneviewrs1064797097
scholarrs1064797097
googlers1064797097
pharmgkbrs1064797097
gwascentralrs1064797097
openSNPrs1064797097
23andMers1064797097
23andMe allrs1064797097
SNPshotrs1064797097
SNPdbers1064797097
MSV3drs1064797097
GWAS Ctlgrs1064797097
Max Magnitude0
ClinVar
Risk rs1064797097(-;-)
Alt rs1064797097(-;-)
Reference Rs1064797097(A;A)
Significance Pathogenic
Disease Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold
Variation info
Gene PPM1D
CLNDBN Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold
Reversed 0
HGVS NC_000017.10:g.58734158delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000488009.1,