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rs587776625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCAGGAC;CCAGGAC) 0 common in clinvar
Make rs587776625(-;-)
Make rs587776625(-;CAGGACC)
Make rs587776625(CAGGACC;CAGGACC)
ReferenceGRCh38 38.1/142
Chromosome16
Position57654104
GeneGPR56
is asnp
is mentioned by
dbSNPrs587776625
ebirs587776625
HLIrs587776625
Exacrs587776625
Varsomers587776625
Maprs587776625
PheGenIrs587776625
hapmaprs587776625
1000 genomesrs587776625
hgdprs587776625
ensemblrs587776625
gopubmedrs587776625
geneviewrs587776625
scholarrs587776625
googlers587776625
pharmgkbrs587776625
gwascentralrs587776625
openSNPrs587776625
23andMers587776625
23andMe allrs587776625
SNP Nexus

SNPshotrs587776625
SNPdbers587776625
MSV3drs587776625
GWAS Ctlgrs587776625
Max Magnitude0
ClinVar
Risk rs587776625(;)
Alt rs587776625(;)
Reference rs587776625(CCAGGAC;CCAGGAC)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57688016_57688022delCAGGACC
CLNSRC OMIM Allelic Variant
CLNACC RCV000006184.4,