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rs532188689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs532188689(C;C)
Make rs532188689(C;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position57654133
GeneGPR56
is asnp
is mentioned by
dbSNPrs532188689
ebirs532188689
HLIrs532188689
Exacrs532188689
Varsomers532188689
Maprs532188689
PheGenIrs532188689
hapmaprs532188689
1000 genomesrs532188689
hgdprs532188689
ensemblrs532188689
gopubmedrs532188689
geneviewrs532188689
scholarrs532188689
googlers532188689
pharmgkbrs532188689
gwascentralrs532188689
openSNPrs532188689
23andMers532188689
23andMe allrs532188689
SNP Nexus

SNPshotrs532188689
SNPdbers532188689
MSV3drs532188689
GWAS Ctlgrs532188689
Max Magnitude0
ClinVar
Risk rs532188689(C;C)
Alt rs532188689(C;C)
Reference rs532188689(G;G)
Significance Probable-Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57688045G>C
CLNSRC ClinVar University of Chicago
CLNACC RCV000146059.1,