rs797044884
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs797044884(-;GA) |
Make rs797044884(GA;GA) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 59677130 |
Gene | CLTC |
is a | snp |
is | mentioned by |
dbSNP | rs797044884 |
dbSNP (classic) | rs797044884 |
ClinGen | rs797044884 |
ebi | rs797044884 |
HLI | rs797044884 |
Exac | rs797044884 |
Gnomad | rs797044884 |
Varsome | rs797044884 |
LitVar | rs797044884 |
Map | rs797044884 |
PheGenI | rs797044884 |
Biobank | rs797044884 |
1000 genomes | rs797044884 |
hgdp | rs797044884 |
ensembl | rs797044884 |
geneview | rs797044884 |
scholar | rs797044884 |
rs797044884 | |
pharmgkb | rs797044884 |
gwascentral | rs797044884 |
openSNP | rs797044884 |
23andMe | rs797044884 |
SNPshot | rs797044884 |
SNPdbe | rs797044884 |
MSV3d | rs797044884 |
GWAS Ctlg | rs797044884 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797044884(AG;AG) |
Alt | rs797044884(AG;AG) |
Reference | Rs797044884(-;-) |
Significance | Probable-Pathogenic |
Disease | Inborn genetic diseases |
Variation | info |
Gene | CLTC |
CLNDBN | Inborn genetic diseases |
Reversed | 0 |
HGVS | NC_000017.10:g.57754490_57754491dupGA |
CLNSRC | |
CLNACC | RCV000190705.1, |