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rs6923492

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs6923492(C;C)
Make rs6923492(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position146434188
GeneGRM1
is asnp
is mentioned by
dbSNPrs6923492
ebirs6923492
HLIrs6923492
Exacrs6923492
Varsomers6923492
Maprs6923492
PheGenIrs6923492
hapmaprs6923492
1000 genomesrs6923492
hgdprs6923492
ensemblrs6923492
gopubmedrs6923492
geneviewrs6923492
scholarrs6923492
googlers6923492
pharmgkbrs6923492
gwascentralrs6923492
openSNPrs6923492
23andMers6923492
23andMe allrs6923492
SNP Nexus

SNPshotrs6923492
SNPdbers6923492
MSV3drs6923492
GWAS Ctlgrs6923492
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 24442360] Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders


ClinVar
Risk rs6923492(C;C)
Alt rs6923492(C;C)
Reference rs6923492(T;T)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene GRM1
CLNDBN not specified
Reversed 0
HGVS NC_000006.11:g.146755324T>C
CLNSRC ClinVar University of Chicago
CLNACC RCV000117205.2,