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rs587783657

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783657(A;A)
Make rs587783657(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position57663470
GeneADGRG1, LOC105371292
is asnp
is mentioned by
dbSNPrs587783657
ebirs587783657
HLIrs587783657
Exacrs587783657
Varsomers587783657
Maprs587783657
PheGenIrs587783657
hapmaprs587783657
1000 genomesrs587783657
hgdprs587783657
ensemblrs587783657
gopubmedrs587783657
geneviewrs587783657
scholarrs587783657
googlers587783657
pharmgkbrs587783657
gwascentralrs587783657
openSNPrs587783657
23andMers587783657
23andMe allrs587783657
SNP Nexus

SNPshotrs587783657
SNPdbers587783657
MSV3drs587783657
GWAS Ctlgrs587783657
Max Magnitude0
ClinVar
Risk rs587783657(A;A)
Alt rs587783657(A;A)
Reference rs587783657(G;G)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57697382G>A
CLNSRC
CLNACC RCV000146049.1,