rs773073663
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs773073663(C;T) |
Make rs773073663(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 127819899 |
Gene | ENG, LOC102723566 |
is a | snp |
is | mentioned by |
dbSNP | rs773073663 |
dbSNP (classic) | rs773073663 |
ClinGen | rs773073663 |
ebi | rs773073663 |
HLI | rs773073663 |
Exac | rs773073663 |
Gnomad | rs773073663 |
Varsome | rs773073663 |
LitVar | rs773073663 |
Map | rs773073663 |
PheGenI | rs773073663 |
Biobank | rs773073663 |
1000 genomes | rs773073663 |
hgdp | rs773073663 |
ensembl | rs773073663 |
geneview | rs773073663 |
scholar | rs773073663 |
rs773073663 | |
pharmgkb | rs773073663 |
gwascentral | rs773073663 |
openSNP | rs773073663 |
23andMe | rs773073663 |
SNPshot | rs773073663 |
SNPdbe | rs773073663 |
MSV3d | rs773073663 |
GWAS Ctlg | rs773073663 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773073663(A;A) rs773073663(T;T) |
Alt | rs773073663(A;A) rs773073663(T;T) |
Reference | Rs773073663(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ENG LOC102723566 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.130582178C>T |
CLNSRC | |
CLNACC | RCV000196088.1, |