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rs587783652

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783652(C;T)
Make rs587783652(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position57659534
GeneADGRG1
is asnp
is mentioned by
dbSNPrs587783652
ebirs587783652
HLIrs587783652
Exacrs587783652
Varsomers587783652
Maprs587783652
PheGenIrs587783652
hapmaprs587783652
1000 genomesrs587783652
hgdprs587783652
ensemblrs587783652
gopubmedrs587783652
geneviewrs587783652
scholarrs587783652
googlers587783652
pharmgkbrs587783652
gwascentralrs587783652
openSNPrs587783652
23andMers587783652
23andMe allrs587783652
SNP Nexus

SNPshotrs587783652
SNPdbers587783652
MSV3drs587783652
GWAS Ctlgrs587783652
Max Magnitude0
ClinVar
Risk rs587783652(T;T)
Alt rs587783652(T;T)
Reference rs587783652(C;C)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57693446C>T
CLNSRC Courtagen Life Sciences
CLNACC RCV000146038.2,