rs747651923
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TATT;TATT) | 0 | common in clinvar |
Make rs747651923(-;-) |
Make rs747651923(-;TATT) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 49471092 |
Gene | ERCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs747651923 |
dbSNP (classic) | rs747651923 |
ClinGen | rs747651923 |
ebi | rs747651923 |
HLI | rs747651923 |
Exac | rs747651923 |
Gnomad | rs747651923 |
Varsome | rs747651923 |
LitVar | rs747651923 |
Map | rs747651923 |
PheGenI | rs747651923 |
Biobank | rs747651923 |
1000 genomes | rs747651923 |
hgdp | rs747651923 |
ensembl | rs747651923 |
geneview | rs747651923 |
scholar | rs747651923 |
rs747651923 | |
pharmgkb | rs747651923 |
gwascentral | rs747651923 |
openSNP | rs747651923 |
23andMe | rs747651923 |
SNPshot | rs747651923 |
SNPdbe | rs747651923 |
MSV3d | rs747651923 |
GWAS Ctlg | rs747651923 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs747651923(-;-) |
Alt | rs747651923(-;-) |
Reference | Rs747651923(TATT;TATT) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ERCC6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.50679138_50679141delTATT |
CLNSRC | |
CLNACC | RCV000494454.1, |