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rs397515320

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515320(-;-)
Make rs397515320(-;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position33442990
GeneSYNGAP1
is asnp
is mentioned by
dbSNPrs397515320
ebirs397515320
HLIrs397515320
Exacrs397515320
Varsomers397515320
Maprs397515320
PheGenIrs397515320
hapmaprs397515320
1000 genomesrs397515320
hgdprs397515320
ensemblrs397515320
gopubmedrs397515320
geneviewrs397515320
scholarrs397515320
googlers397515320
pharmgkbrs397515320
gwascentralrs397515320
openSNPrs397515320
23andMers397515320
23andMe allrs397515320
SNP Nexus

SNPshotrs397515320
SNPdbers397515320
MSV3drs397515320
GWAS Ctlgrs397515320
Max Magnitude0
ClinVar
Risk rs397515320(;)
Alt rs397515320(;)
Reference rs397515320(T;T)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene SYNGAP1
CLNDBN Mental retardation, autosomal dominant 5
Reversed 0
HGVS NC_000006.11:g.33410767delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000006766.3,