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rs121908462

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908462(C;T)
Make rs121908462(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position57651247
GeneGPR56
is asnp
is mentioned by
dbSNPrs121908462
ebirs121908462
HLIrs121908462
Exacrs121908462
Varsomers121908462
Maprs121908462
PheGenIrs121908462
hapmaprs121908462
1000 genomesrs121908462
hgdprs121908462
ensemblrs121908462
gopubmedrs121908462
geneviewrs121908462
scholarrs121908462
googlers121908462
pharmgkbrs121908462
gwascentralrs121908462
openSNPrs121908462
23andMers121908462
23andMe allrs121908462
SNP Nexus

SNPshotrs121908462
SNPdbers121908462
MSV3drs121908462
GWAS Ctlgrs121908462
Max Magnitude0
OMIM604110
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908462(T;T)
Alt rs121908462(T;T)
Reference rs121908462(C;C)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57685159C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006185.3,