rs760933323
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TT;TT) | 0 | common in clinvar |
Make rs760933323(-;-) |
Make rs760933323(-;TT) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 76733583 |
Gene | METTL23 |
is a | snp |
is | mentioned by |
dbSNP | rs760933323 |
dbSNP (classic) | rs760933323 |
ClinGen | rs760933323 |
ebi | rs760933323 |
HLI | rs760933323 |
Exac | rs760933323 |
Gnomad | rs760933323 |
Varsome | rs760933323 |
LitVar | rs760933323 |
Map | rs760933323 |
PheGenI | rs760933323 |
Biobank | rs760933323 |
1000 genomes | rs760933323 |
hgdp | rs760933323 |
ensembl | rs760933323 |
geneview | rs760933323 |
scholar | rs760933323 |
rs760933323 | |
pharmgkb | rs760933323 |
gwascentral | rs760933323 |
openSNP | rs760933323 |
23andMe | rs760933323 |
SNPshot | rs760933323 |
SNPdbe | rs760933323 |
MSV3d | rs760933323 |
GWAS Ctlg | rs760933323 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs760933323(-;-) |
Alt | rs760933323(-;-) |
Reference | Rs760933323(TT;TT) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | METTL23 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.74729665_74729666delTT |
CLNSRC | |
CLNACC | RCV000486806.1, |