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rs786204777

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204777(C;T)
Make rs786204777(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position57650297
GeneADGRG1
is asnp
is mentioned by
dbSNPrs786204777
dbSNP (classic)rs786204777
ClinGenrs786204777
ebirs786204777
HLIrs786204777
Exacrs786204777
Gnomadrs786204777
Varsomers786204777
LitVarrs786204777
Maprs786204777
PheGenIrs786204777
Biobankrs786204777
1000 genomesrs786204777
hgdprs786204777
ensemblrs786204777
geneviewrs786204777
scholarrs786204777
googlers786204777
pharmgkbrs786204777
gwascentralrs786204777
openSNPrs786204777
23andMers786204777
SNPshotrs786204777
SNPdbers786204777
MSV3drs786204777
GWAS Ctlgrs786204777
Max Magnitude0
ClinVar
Risk rs786204777(T;T)
Alt rs786204777(T;T)
Reference Rs786204777(C;C)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal
Reversed 0
HGVS NC_000016.9:g.57684209C>T
CLNSRC
CLNACC RCV000169661.1,