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rs1064797322

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome6
Position33435306
GeneSYNGAP1
is asnp
is mentioned by
dbSNPrs1064797322
dbSNP (old)rs1064797322
ClinGenrs1064797322
ebirs1064797322
HLIrs1064797322
Exacrs1064797322
Gnomadrs1064797322
Varsomers1064797322
Maprs1064797322
PheGenIrs1064797322
Biobankrs1064797322
1000 genomesrs1064797322
hgdprs1064797322
ensemblrs1064797322
gopubmedrs1064797322
geneviewrs1064797322
scholarrs1064797322
googlers1064797322
pharmgkbrs1064797322
gwascentralrs1064797322
openSNPrs1064797322
23andMers1064797322
23andMe allrs1064797322
SNPshotrs1064797322
SNPdbers1064797322
MSV3drs1064797322
GWAS Ctlgrs1064797322
Max Magnitude0
ClinVar
Risk rs1064797322(A;A)
Alt rs1064797322(A;A)
Reference Rs1064797322(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SYNGAP1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.33403083G>A
CLNSRC
CLNACC RCV000488038.1,