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rs587780473

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780473(-;-)
Make rs587780473(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position33440835
GeneSYNGAP1
is asnp
is mentioned by
dbSNPrs587780473
ebirs587780473
HLIrs587780473
Exacrs587780473
Varsomers587780473
Maprs587780473
PheGenIrs587780473
hapmaprs587780473
1000 genomesrs587780473
hgdprs587780473
ensemblrs587780473
gopubmedrs587780473
geneviewrs587780473
scholarrs587780473
googlers587780473
pharmgkbrs587780473
gwascentralrs587780473
openSNPrs587780473
23andMers587780473
23andMe allrs587780473
SNP Nexus

SNPshotrs587780473
SNPdbers587780473
MSV3drs587780473
GWAS Ctlgrs587780473
Max Magnitude0
ClinVar
Risk rs587780473(;)
Alt rs587780473(;)
Reference rs587780473(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene SYNGAP1
CLNDBN Mental retardation, autosomal dominant 5
Reversed 0
HGVS NC_000006.11:g.33408612delC
CLNSRC
CLNACC RCV000118565.3,