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

rs1064795331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome6
Position33440769
GeneSYNGAP1
is asnp
is mentioned by
dbSNPrs1064795331
dbSNP (old)rs1064795331
ClinGenrs1064795331
ebirs1064795331
HLIrs1064795331
Exacrs1064795331
Gnomadrs1064795331
Varsomers1064795331
Maprs1064795331
PheGenIrs1064795331
Biobankrs1064795331
1000 genomesrs1064795331
hgdprs1064795331
ensemblrs1064795331
gopubmedrs1064795331
geneviewrs1064795331
scholarrs1064795331
googlers1064795331
pharmgkbrs1064795331
gwascentralrs1064795331
openSNPrs1064795331
23andMers1064795331
23andMe allrs1064795331
SNPshotrs1064795331
SNPdbers1064795331
MSV3drs1064795331
GWAS Ctlgrs1064795331
Max Magnitude0
ClinVar
Risk rs1064795331(T;T)
Alt rs1064795331(T;T)
Reference Rs1064795331(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SYNGAP1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.33408546C>T
CLNSRC
CLNACC RCV000483715.1,