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rs1085307871

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 8.8 Mental retardation, type 5; SYNGAP1-related
Make rs1085307871(T;T)
Chromosome6
Position33432769
GeneSYNGAP1
is asnp
is mentioned by
dbSNPrs1085307871
dbSNP (old)rs1085307871
ClinGenrs1085307871
ebirs1085307871
HLIrs1085307871
Exacrs1085307871
Gnomadrs1085307871
Varsomers1085307871
Maprs1085307871
PheGenIrs1085307871
Biobankrs1085307871
1000 genomesrs1085307871
hgdprs1085307871
ensemblrs1085307871
gopubmedrs1085307871
geneviewrs1085307871
scholarrs1085307871
googlers1085307871
pharmgkbrs1085307871
gwascentralrs1085307871
openSNPrs1085307871
23andMers1085307871
23andMe allrs1085307871
SNPshotrs1085307871
SNPdbers1085307871
MSV3drs1085307871
GWAS Ctlgrs1085307871
Max Magnitude8.8
ClinVar
Risk rs1085307871(T;T)
Alt rs1085307871(T;T)
Reference Rs1085307871(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SYNGAP1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.33400546C>T
CLNSRC
CLNACC RCV000489135.1,