rs74810894
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs74810894(C;C) |
Make rs74810894(C;G) |
Make rs74810894(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 9 |
Position | 35657891 |
Gene | CCDC107, RMRP |
is a | snp |
is | mentioned by |
dbSNP | rs74810894 |
dbSNP (classic) | rs74810894 |
ClinGen | rs74810894 |
ebi | rs74810894 |
HLI | rs74810894 |
Exac | rs74810894 |
Gnomad | rs74810894 |
Varsome | rs74810894 |
LitVar | rs74810894 |
Map | rs74810894 |
PheGenI | rs74810894 |
Biobank | rs74810894 |
1000 genomes | rs74810894 |
hgdp | rs74810894 |
ensembl | rs74810894 |
geneview | rs74810894 |
scholar | rs74810894 |
rs74810894 | |
pharmgkb | rs74810894 |
gwascentral | rs74810894 |
openSNP | rs74810894 |
23andMe | rs74810894 |
SNPshot | rs74810894 |
SNPdbe | rs74810894 |
MSV3d | rs74810894 |
GWAS Ctlg | rs74810894 |
Max Magnitude | 0 |
[PMID 27569544] 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.