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

rs74810894

From SNPedia

Orientationplus
Stabilizedplus
Make rs74810894(C;C)
Make rs74810894(C;G)
Make rs74810894(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position35657891
GeneCCDC107, RMRP
is asnp
is mentioned by
dbSNPrs74810894
dbSNP (classic)rs74810894
ClinGenrs74810894
ebirs74810894
HLIrs74810894
Exacrs74810894
Gnomadrs74810894
Varsomers74810894
LitVarrs74810894
Maprs74810894
PheGenIrs74810894
Biobankrs74810894
1000 genomesrs74810894
hgdprs74810894
ensemblrs74810894
geneviewrs74810894
scholarrs74810894
googlers74810894
pharmgkbrs74810894
gwascentralrs74810894
openSNPrs74810894
23andMers74810894
SNPshotrs74810894
SNPdbers74810894
MSV3drs74810894
GWAS Ctlgrs74810894
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.