rs796052758
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs796052758(-;-) |
Make rs796052758(-;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 18122381 |
Gene | NHLRC1 |
is a | snp |
is | mentioned by |
dbSNP | rs796052758 |
dbSNP (classic) | rs796052758 |
ClinGen | rs796052758 |
ebi | rs796052758 |
HLI | rs796052758 |
Exac | rs796052758 |
Gnomad | rs796052758 |
Varsome | rs796052758 |
LitVar | rs796052758 |
Map | rs796052758 |
PheGenI | rs796052758 |
Biobank | rs796052758 |
1000 genomes | rs796052758 |
hgdp | rs796052758 |
ensembl | rs796052758 |
geneview | rs796052758 |
scholar | rs796052758 |
rs796052758 | |
pharmgkb | rs796052758 |
gwascentral | rs796052758 |
openSNP | rs796052758 |
23andMe | rs796052758 |
SNPshot | rs796052758 |
SNPdbe | rs796052758 |
MSV3d | rs796052758 |
GWAS Ctlg | rs796052758 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052758(-;-) |
Alt | rs796052758(-;-) |
Reference | Rs796052758(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | NHLRC1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000006.11:g.18122612delG |
CLNSRC | |
CLNACC | RCV000188218.1, |