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rs121908463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908463(A;A)
Make rs121908463(A;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position57656244
GeneGPR56
is asnp
is mentioned by
dbSNPrs121908463
ebirs121908463
HLIrs121908463
Exacrs121908463
Varsomers121908463
Maprs121908463
PheGenIrs121908463
hapmaprs121908463
1000 genomesrs121908463
hgdprs121908463
ensemblrs121908463
gopubmedrs121908463
geneviewrs121908463
scholarrs121908463
googlers121908463
pharmgkbrs121908463
gwascentralrs121908463
openSNPrs121908463
23andMers121908463
23andMe allrs121908463
SNP Nexus

SNPshotrs121908463
SNPdbers121908463
MSV3drs121908463
GWAS Ctlgrs121908463
Max Magnitude0
OMIM604110
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908463(A;A)
Alt rs121908463(A;A)
Reference rs121908463(T;T)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57690156T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006186.3,