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rs121908464

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908464(C;T)
Make rs121908464(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position57661707
GeneGPR56
is asnp
is mentioned by
dbSNPrs121908464
ebirs121908464
HLIrs121908464
Exacrs121908464
Varsomers121908464
Maprs121908464
PheGenIrs121908464
hapmaprs121908464
1000 genomesrs121908464
hgdprs121908464
ensemblrs121908464
gopubmedrs121908464
geneviewrs121908464
scholarrs121908464
googlers121908464
pharmgkbrs121908464
gwascentralrs121908464
openSNPrs121908464
23andMers121908464
23andMe allrs121908464
SNP Nexus

SNPshotrs121908464
SNPdbers121908464
MSV3drs121908464
GWAS Ctlgrs121908464
Max Magnitude0
OMIM604110
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908464(T;T)
Alt rs121908464(T;T)
Reference rs121908464(C;C)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57695619C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006187.3,