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rs769262495

From SNPedia

Orientationplus
Stabilizedplus
Make rs769262495(A;A)
Make rs769262495(A;C)
Make rs769262495(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome8
Position11703355
GeneGATA4
is asnp
is mentioned by
dbSNPrs769262495
dbSNP (classic)rs769262495
ClinGenrs769262495
ebirs769262495
HLIrs769262495
Exacrs769262495
Gnomadrs769262495
Varsomers769262495
LitVarrs769262495
Maprs769262495
PheGenIrs769262495
Biobankrs769262495
1000 genomesrs769262495
hgdprs769262495
ensemblrs769262495
geneviewrs769262495
scholarrs769262495
googlers769262495
pharmgkbrs769262495
gwascentralrs769262495
openSNPrs769262495
23andMers769262495
23andMe allrs769262495
SNPshotrs769262495
SNPdbers769262495
MSV3drs769262495
GWAS Ctlgrs769262495
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.