Have questions? Visit https://www.reddit.com/r/SNPedia

rs191615506

From SNPedia

Orientationplus
Stabilizedplus
Make rs191615506(A;A)
Make rs191615506(A;G)
Make rs191615506(G;G)
ReferenceGRCh38.p7 38.3/149
ChromosomeX
Position38352331
GeneOTC
is asnp
is mentioned by
dbSNPrs191615506
dbSNP (classic)rs191615506
ClinGenrs191615506
ebirs191615506
HLIrs191615506
Exacrs191615506
Gnomadrs191615506
Varsomers191615506
LitVarrs191615506
Maprs191615506
PheGenIrs191615506
Biobankrs191615506
1000 genomesrs191615506
hgdprs191615506
ensemblrs191615506
geneviewrs191615506
scholarrs191615506
googlers191615506
pharmgkbrs191615506
gwascentralrs191615506
openSNPrs191615506
23andMers191615506
23andMe allrs191615506
SNPshotrs191615506
SNPdbers191615506
MSV3drs191615506
GWAS Ctlgrs191615506
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.