rs1057518014
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CCCTC;CCCTC) | 0 | common in clinvar |
Make rs1057518014(-;-) |
Make rs1057518014(-;CCCTC) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 8 |
Position | 143817103 |
Gene | PUF60, SCRIB |
is a | snp |
is | mentioned by |
dbSNP | rs1057518014 |
dbSNP (classic) | rs1057518014 |
ClinGen | rs1057518014 |
ebi | rs1057518014 |
HLI | rs1057518014 |
Exac | rs1057518014 |
Gnomad | rs1057518014 |
Varsome | rs1057518014 |
LitVar | rs1057518014 |
Map | rs1057518014 |
PheGenI | rs1057518014 |
Biobank | rs1057518014 |
1000 genomes | rs1057518014 |
hgdp | rs1057518014 |
ensembl | rs1057518014 |
geneview | rs1057518014 |
scholar | rs1057518014 |
rs1057518014 | |
pharmgkb | rs1057518014 |
gwascentral | rs1057518014 |
openSNP | rs1057518014 |
23andMe | rs1057518014 |
SNPshot | rs1057518014 |
SNPdbe | rs1057518014 |
MSV3d | rs1057518014 |
GWAS Ctlg | rs1057518014 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057518014(-;-) |
Alt | rs1057518014(-;-) |
Reference | Rs1057518014(CCCTC;CCCTC) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PUF60 SCRIB |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000008.10:g.144899273_144899277delGAGGG |
CLNSRC | |
CLNACC | RCV000413995.1, |