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rs587776624

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776624(C;C)
Make rs587776624(C;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position57653985
GeneGPR56
is asnp
is mentioned by
dbSNPrs587776624
ebirs587776624
HLIrs587776624
Exacrs587776624
Varsomers587776624
Maprs587776624
PheGenIrs587776624
hapmaprs587776624
1000 genomesrs587776624
hgdprs587776624
ensemblrs587776624
gopubmedrs587776624
geneviewrs587776624
scholarrs587776624
googlers587776624
pharmgkbrs587776624
gwascentralrs587776624
openSNPrs587776624
23andMers587776624
23andMe allrs587776624
SNP Nexus

SNPshotrs587776624
SNPdbers587776624
MSV3drs587776624
GWAS Ctlgrs587776624
Max Magnitude0
ClinVar
Risk rs587776624(C;C)
Alt rs587776624(C;C)
Reference rs587776624(G;G)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57687897G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006183.3,