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rs587783656

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783656(C;C)
Make rs587783656(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position57661882
GeneADGRG1, LOC105371292
is asnp
is mentioned by
dbSNPrs587783656
ebirs587783656
HLIrs587783656
Exacrs587783656
Varsomers587783656
Maprs587783656
PheGenIrs587783656
hapmaprs587783656
1000 genomesrs587783656
hgdprs587783656
ensemblrs587783656
gopubmedrs587783656
geneviewrs587783656
scholarrs587783656
googlers587783656
pharmgkbrs587783656
gwascentralrs587783656
openSNPrs587783656
23andMers587783656
23andMe allrs587783656
SNP Nexus

SNPshotrs587783656
SNPdbers587783656
MSV3drs587783656
GWAS Ctlgrs587783656
Max Magnitude0
ClinVar
Risk rs587783656(C;C)
Alt rs587783656(C;C)
Reference rs587783656(G;G)
Significance Probable-Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57695794G>C
CLNSRC
CLNACC RCV000146047.1,