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rs146278035

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146278035(C;T)
Make rs146278035(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position57651421
GeneGPR56
is asnp
is mentioned by
dbSNPrs146278035
ebirs146278035
HLIrs146278035
Exacrs146278035
Varsomers146278035
Maprs146278035
PheGenIrs146278035
hapmaprs146278035
1000 genomesrs146278035
hgdprs146278035
ensemblrs146278035
gopubmedrs146278035
geneviewrs146278035
scholarrs146278035
googlers146278035
pharmgkbrs146278035
gwascentralrs146278035
openSNPrs146278035
23andMers146278035
23andMe allrs146278035
SNP Nexus

SNPshotrs146278035
SNPdbers146278035
MSV3drs146278035
GWAS Ctlgrs146278035
Max Magnitude0
ClinVar
Risk rs146278035(T;T)
Alt rs146278035(T;T)
Reference rs146278035(C;C)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57685333C>T
CLNSRC ClinVar University of Chicago
CLNACC RCV000146051.1,