rs753962912
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TA;TA) | 0 | common in clinvar |
Make rs753962912(-;-) |
Make rs753962912(-;TA) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 13 |
Position | 51964995 |
Gene | ATP7B |
is a | snp |
is | mentioned by |
dbSNP | rs753962912 |
dbSNP (classic) | rs753962912 |
ClinGen | rs753962912 |
ebi | rs753962912 |
HLI | rs753962912 |
Exac | rs753962912 |
Gnomad | rs753962912 |
Varsome | rs753962912 |
LitVar | rs753962912 |
Map | rs753962912 |
PheGenI | rs753962912 |
Biobank | rs753962912 |
1000 genomes | rs753962912 |
hgdp | rs753962912 |
ensembl | rs753962912 |
geneview | rs753962912 |
scholar | rs753962912 |
rs753962912 | |
pharmgkb | rs753962912 |
gwascentral | rs753962912 |
openSNP | rs753962912 |
23andMe | rs753962912 |
SNPshot | rs753962912 |
SNPdbe | rs753962912 |
MSV3d | rs753962912 |
GWAS Ctlg | rs753962912 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs753962912(-;-) |
Alt | rs753962912(-;-) |
Reference | Rs753962912(TA;TA) |
Significance | Other |
Disease | Wilson disease |
Variation | info |
Gene | ATP7B |
CLNDBN | Wilson disease |
Reversed | 0 |
HGVS | NC_000013.10:g.52539131_52539132delTA |
CLNSRC | |
CLNACC | RCV000169524.2, |