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rs141875471

From SNPedia

Orientationplus
Stabilizedplus
Make rs141875471(A;A)
Make rs141875471(A;G)
Make rs141875471(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position114266710
is asnp
is mentioned by
dbSNPrs141875471
dbSNP (old)rs141875471
ClinGenrs141875471
ebirs141875471
HLIrs141875471
Exacrs141875471
Gnomadrs141875471
Varsomers141875471
Maprs141875471
PheGenIrs141875471
Biobankrs141875471
1000 genomesrs141875471
hgdprs141875471
ensemblrs141875471
gopubmedrs141875471
geneviewrs141875471
scholarrs141875471
googlers141875471
pharmgkbrs141875471
gwascentralrs141875471
openSNPrs141875471
23andMers141875471
23andMe allrs141875471
SNPshotrs141875471
SNPdbers141875471
MSV3drs141875471
GWAS Ctlgrs141875471
Max Magnitude

[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.