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rs587783654

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783654(C;C)
Make rs587783654(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position57659616
GeneADGRG1
is asnp
is mentioned by
dbSNPrs587783654
ebirs587783654
HLIrs587783654
Exacrs587783654
Varsomers587783654
Maprs587783654
PheGenIrs587783654
hapmaprs587783654
1000 genomesrs587783654
hgdprs587783654
ensemblrs587783654
gopubmedrs587783654
geneviewrs587783654
scholarrs587783654
googlers587783654
pharmgkbrs587783654
gwascentralrs587783654
openSNPrs587783654
23andMers587783654
23andMe allrs587783654
SNP Nexus

SNPshotrs587783654
SNPdbers587783654
MSV3drs587783654
GWAS Ctlgrs587783654
Max Magnitude0
ClinVar
Risk rs587783654(C;C)
Alt rs587783654(C;C)
Reference rs587783654(T;T)
Significance Probable-Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57693528T>C
CLNSRC
CLNACC RCV000146041.1,