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rs532876832

From SNPedia

Orientationplus
Stabilizedplus
Make rs532876832(A;A)
Make rs532876832(A;G)
Make rs532876832(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome21
Position25881337
GeneAPP
is asnp
is mentioned by
dbSNPrs532876832
dbSNP (classic)rs532876832
ClinGenrs532876832
ebirs532876832
HLIrs532876832
Exacrs532876832
Gnomadrs532876832
Varsomers532876832
LitVarrs532876832
Maprs532876832
PheGenIrs532876832
Biobankrs532876832
1000 genomesrs532876832
hgdprs532876832
ensemblrs532876832
geneviewrs532876832
scholarrs532876832
googlers532876832
pharmgkbrs532876832
gwascentralrs532876832
openSNPrs532876832
23andMers532876832
23andMe allrs532876832
SNPshotrs532876832
SNPdbers532876832
MSV3drs532876832
GWAS Ctlgrs532876832
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.