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rs797045602

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045602(-;TT)
Make rs797045602(TT;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position57655920
GeneADGRG1
is asnp
is mentioned by
dbSNPrs797045602
dbSNP (old)rs797045602
ClinGenrs797045602
ebirs797045602
HLIrs797045602
Exacrs797045602
Gnomadrs797045602
Varsomers797045602
Maprs797045602
PheGenIrs797045602
Biobankrs797045602
1000 genomesrs797045602
hgdprs797045602
ensemblrs797045602
gopubmedrs797045602
geneviewrs797045602
scholarrs797045602
googlers797045602
pharmgkbrs797045602
gwascentralrs797045602
openSNPrs797045602
23andMers797045602
23andMe allrs797045602
SNP Nexus

SNPshotrs797045602
SNPdbers797045602
MSV3drs797045602
GWAS Ctlgrs797045602
Max Magnitude0
ClinVar
Risk rs797045602(TT;TT)
Alt rs797045602(TT;TT)
Reference Rs797045602(-;-)
Significance Pathogenic
Disease Polymicrogyria not provided
Variation info
Gene ADGRG1 GPR56
CLNDBN Polymicrogyria, bilateral frontoparietal not provided
Reversed 0
HGVS NC_000016.9:g.57689831_57689832dupTT
CLNSRC
CLNACC RCV000193721.1, RCV000482949.1,