rs375554612
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs375554612(-;-) |
Make rs375554612(-;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 13 |
Position | 108209365 |
Gene | LIG4 |
is a | snp |
is | mentioned by |
dbSNP | rs375554612 |
dbSNP (classic) | rs375554612 |
ClinGen | rs375554612 |
ebi | rs375554612 |
HLI | rs375554612 |
Exac | rs375554612 |
Gnomad | rs375554612 |
Varsome | rs375554612 |
LitVar | rs375554612 |
Map | rs375554612 |
PheGenI | rs375554612 |
Biobank | rs375554612 |
1000 genomes | rs375554612 |
hgdp | rs375554612 |
ensembl | rs375554612 |
geneview | rs375554612 |
scholar | rs375554612 |
rs375554612 | |
pharmgkb | rs375554612 |
gwascentral | rs375554612 |
openSNP | rs375554612 |
23andMe | rs375554612 |
SNPshot | rs375554612 |
SNPdbe | rs375554612 |
MSV3d | rs375554612 |
GWAS Ctlg | rs375554612 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs375554612(-;-) |
Alt | rs375554612(-;-) |
Reference | Rs375554612(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | LIG4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000013.10:g.108861713delT |
CLNSRC | |
CLNACC | RCV000480290.1, |