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rs587776623

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776623(C;C)
Make rs587776623(C;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position57656620
GeneGPR56
is asnp
is mentioned by
dbSNPrs587776623
ebirs587776623
HLIrs587776623
Exacrs587776623
Varsomers587776623
Maprs587776623
PheGenIrs587776623
hapmaprs587776623
1000 genomesrs587776623
hgdprs587776623
ensemblrs587776623
gopubmedrs587776623
geneviewrs587776623
scholarrs587776623
googlers587776623
pharmgkbrs587776623
gwascentralrs587776623
openSNPrs587776623
23andMers587776623
23andMe allrs587776623
SNP Nexus

SNPshotrs587776623
SNPdbers587776623
MSV3drs587776623
GWAS Ctlgrs587776623
Max Magnitude0
ClinVar
Risk rs587776623(C;C)
Alt rs587776623(C;C)
Reference rs587776623(G;G)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57690532G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006182.3,