rs797044565
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CAGT;CAGT) | 0 | common in clinvar |
Make rs797044565(-;-) |
Make rs797044565(-;CAGT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 118503457 |
Gene | KMT2A |
is a | snp |
is | mentioned by |
dbSNP | rs797044565 |
dbSNP (classic) | rs797044565 |
ClinGen | rs797044565 |
ebi | rs797044565 |
HLI | rs797044565 |
Exac | rs797044565 |
Gnomad | rs797044565 |
Varsome | rs797044565 |
LitVar | rs797044565 |
Map | rs797044565 |
PheGenI | rs797044565 |
Biobank | rs797044565 |
1000 genomes | rs797044565 |
hgdp | rs797044565 |
ensembl | rs797044565 |
geneview | rs797044565 |
scholar | rs797044565 |
rs797044565 | |
pharmgkb | rs797044565 |
gwascentral | rs797044565 |
openSNP | rs797044565 |
23andMe | rs797044565 |
SNPshot | rs797044565 |
SNPdbe | rs797044565 |
MSV3d | rs797044565 |
GWAS Ctlg | rs797044565 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797044565(-;-) |
Alt | rs797044565(-;-) |
Reference | Rs797044565(CAGT;CAGT) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | KMT2A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.118374172_118374175delCAGT |
CLNSRC | |
CLNACC | RCV000171465.1, |