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rs786205649

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205649(-;-)
Make rs786205649(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position33435176
GeneSYNGAP1
is asnp
is mentioned by
dbSNPrs786205649
ebirs786205649
HLIrs786205649
Exacrs786205649
Varsomers786205649
Maprs786205649
PheGenIrs786205649
hapmaprs786205649
1000 genomesrs786205649
hgdprs786205649
ensemblrs786205649
gopubmedrs786205649
geneviewrs786205649
scholarrs786205649
googlers786205649
pharmgkbrs786205649
gwascentralrs786205649
openSNPrs786205649
23andMers786205649
23andMe allrs786205649
SNP Nexus

SNPshotrs786205649
SNPdbers786205649
MSV3drs786205649
GWAS Ctlgrs786205649
Max Magnitude0
ClinVar
Risk rs786205649(;)
Alt rs786205649(;)
Reference rs786205649(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SYNGAP1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.33402953delG
CLNSRC
CLNACC RCV000171521.1,