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rs756994701

From SNPedia

Orientationplus
Stabilizedplus
Make rs756994701(A;A)
Make rs756994701(A;G)
Make rs756994701(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position127854365
GeneENG
is asnp
is mentioned by
dbSNPrs756994701
dbSNP (classic)rs756994701
ClinGenrs756994701
ebirs756994701
HLIrs756994701
Exacrs756994701
Gnomadrs756994701
Varsomers756994701
LitVarrs756994701
Maprs756994701
PheGenIrs756994701
Biobankrs756994701
1000 genomesrs756994701
hgdprs756994701
ensemblrs756994701
geneviewrs756994701
scholarrs756994701
googlers756994701
pharmgkbrs756994701
gwascentralrs756994701
openSNPrs756994701
23andMers756994701
SNPshotrs756994701
SNPdbers756994701
MSV3drs756994701
GWAS Ctlgrs756994701
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.