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rs1057518178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 8.8 Mental retardation, type 5; SYNGAP1-related
(G;G) 0 common in clinvar


Make rs1057518178(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position33440768
GeneSYNGAP1
is asnp
is mentioned by
dbSNPrs1057518178
dbSNP (old)rs1057518178
ClinGenrs1057518178
ebirs1057518178
HLIrs1057518178
Exacrs1057518178
Gnomadrs1057518178
Varsomers1057518178
Maprs1057518178
PheGenIrs1057518178
Biobankrs1057518178
1000 genomesrs1057518178
hgdprs1057518178
ensemblrs1057518178
gopubmedrs1057518178
geneviewrs1057518178
scholarrs1057518178
googlers1057518178
pharmgkbrs1057518178
gwascentralrs1057518178
openSNPrs1057518178
23andMers1057518178
23andMe allrs1057518178
SNPshotrs1057518178
SNPdbers1057518178
MSV3drs1057518178
GWAS Ctlgrs1057518178
Max Magnitude8.8
ClinVar
Risk rs1057518178(A;A)
Alt rs1057518178(A;A)
Reference Rs1057518178(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SYNGAP1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.33408545G>A
CLNSRC
CLNACC RCV000412895.1,