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rs587777312

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAACGGTTGCCAGGG;CAACGGTTGCCAGGG) 0 common in clinvar
Make rs587777312(-;-)
Make rs587777312(-;CAACGGTTGCCAGGG)
ReferenceGRCh38 38.1/142
Chromosome16
Position57639389
GeneGPR56
is asnp
is mentioned by
dbSNPrs587777312
ebirs587777312
HLIrs587777312
Exacrs587777312
Varsomers587777312
Maprs587777312
PheGenIrs587777312
hapmaprs587777312
1000 genomesrs587777312
hgdprs587777312
ensemblrs587777312
gopubmedrs587777312
geneviewrs587777312
scholarrs587777312
googlers587777312
pharmgkbrs587777312
gwascentralrs587777312
openSNPrs587777312
23andMers587777312
23andMe allrs587777312
SNP Nexus

SNPshotrs587777312
SNPdbers587777312
MSV3drs587777312
GWAS Ctlgrs587777312
Max Magnitude0
ClinVar
Risk rs587777312(;)
Alt rs587777312(;)
Reference rs587777312(CAACGGTTGCCAGGG;CAACGGTTGCCAGGG)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral perisylvian, autosomal recessive
Reversed 0
HGVS NC_000016.9:g.57673301_57673315delCAACGGTTGCCAGGG
CLNSRC OMIM Allelic Variant
CLNACC RCV000114942.3,