rs121918844
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common/normal |
Make rs121918844(-;T) |
Make rs121918844(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 68444664 |
Gene | RPE65 |
is a | snp |
is | mentioned by |
dbSNP | rs121918844 |
dbSNP (classic) | rs121918844 |
ClinGen | rs121918844 |
ebi | rs121918844 |
HLI | rs121918844 |
Exac | rs121918844 |
Gnomad | rs121918844 |
Varsome | rs121918844 |
LitVar | rs121918844 |
Map | rs121918844 |
PheGenI | rs121918844 |
Biobank | rs121918844 |
1000 genomes | rs121918844 |
hgdp | rs121918844 |
ensembl | rs121918844 |
geneview | rs121918844 |
scholar | rs121918844 |
rs121918844 | |
pharmgkb | rs121918844 |
gwascentral | rs121918844 |
openSNP | rs121918844 |
23andMe | rs121918844 |
SNPshot | rs121918844 |
SNPdbe | rs121918844 |
MSV3d | rs121918844 |
GWAS Ctlg | rs121918844 |
Max Magnitude | 0 |
[PMID 26334176] This SNP is included in a curated list of mutations useful to include on an Ashkenazi Jews screening panel.
aka c.361dupT; Leber congenital amaurosis 2?