rs797044907
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs797044907(-;AGCT) |
Make rs797044907(AGCT;AGCT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 72108662 |
Gene | ANAPC15, LRTOMT |
is a | snp |
is | mentioned by |
dbSNP | rs797044907 |
dbSNP (classic) | rs797044907 |
ClinGen | rs797044907 |
ebi | rs797044907 |
HLI | rs797044907 |
Exac | rs797044907 |
Gnomad | rs797044907 |
Varsome | rs797044907 |
LitVar | rs797044907 |
Map | rs797044907 |
PheGenI | rs797044907 |
Biobank | rs797044907 |
1000 genomes | rs797044907 |
hgdp | rs797044907 |
ensembl | rs797044907 |
geneview | rs797044907 |
scholar | rs797044907 |
rs797044907 | |
pharmgkb | rs797044907 |
gwascentral | rs797044907 |
openSNP | rs797044907 |
23andMe | rs797044907 |
SNPshot | rs797044907 |
SNPdbe | rs797044907 |
MSV3d | rs797044907 |
GWAS Ctlg | rs797044907 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797044907(AGCT;AGCT) |
Alt | rs797044907(AGCT;AGCT) |
Reference | Rs797044907(-;-) |
Significance | Pathogenic |
Disease | Inborn genetic diseases |
Variation | info |
Gene | ANAPC15 LRTOMT |
CLNDBN | Inborn genetic diseases |
Reversed | 0 |
HGVS | NC_000011.9:g.71819708_71819709insAGCT |
CLNSRC | |
CLNACC | RCV000190734.1, |