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rs1064796033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;T) 8.8 Mental retardation, type 5; SYNGAP1-related
(T;T) 0 common in clinvar


Make rs1064796033(-;-)
Chromosome6
Position33443779
GeneSYNGAP1
is asnp
is mentioned by
dbSNPrs1064796033
dbSNP (old)rs1064796033
ClinGenrs1064796033
ebirs1064796033
HLIrs1064796033
Exacrs1064796033
Gnomadrs1064796033
Varsomers1064796033
Maprs1064796033
PheGenIrs1064796033
Biobankrs1064796033
1000 genomesrs1064796033
hgdprs1064796033
ensemblrs1064796033
gopubmedrs1064796033
geneviewrs1064796033
scholarrs1064796033
googlers1064796033
pharmgkbrs1064796033
gwascentralrs1064796033
openSNPrs1064796033
23andMers1064796033
23andMe allrs1064796033
SNPshotrs1064796033
SNPdbers1064796033
MSV3drs1064796033
GWAS Ctlgrs1064796033
Max Magnitude8.8
ClinVar
Risk rs1064796033(-;-)
Alt rs1064796033(-;-)
Reference Rs1064796033(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SYNGAP1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.33411556delT
CLNSRC
CLNACC RCV000481505.1,