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rs766501882

From SNPedia

Orientationplus
Stabilizedplus
Make rs766501882(A;A)
Make rs766501882(A;G)
Make rs766501882(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position171652619
GeneMYOC
is asnp
is mentioned by
dbSNPrs766501882
dbSNP (classic)rs766501882
ClinGenrs766501882
ebirs766501882
HLIrs766501882
Exacrs766501882
Gnomadrs766501882
Varsomers766501882
LitVarrs766501882
Maprs766501882
PheGenIrs766501882
Biobankrs766501882
1000 genomesrs766501882
hgdprs766501882
ensemblrs766501882
geneviewrs766501882
scholarrs766501882
googlers766501882
pharmgkbrs766501882
gwascentralrs766501882
openSNPrs766501882
23andMers766501882
23andMe allrs766501882
SNPshotrs766501882
SNPdbers766501882
MSV3drs766501882
GWAS Ctlgrs766501882
Max Magnitude0

[PMID 27569544OA-icon.png] A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease. This SNP maps to a position listed in Table S6 as a non-coding variant that their biocurators felt was convincingly associated with a Mendelian disease.