rs1057523045
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1057523045(C;G) |
Make rs1057523045(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 7542038 |
Gene | DSP, LOC101928076 |
is a | snp |
is | mentioned by |
dbSNP | rs1057523045 |
dbSNP (classic) | rs1057523045 |
ClinGen | rs1057523045 |
ebi | rs1057523045 |
HLI | rs1057523045 |
Exac | rs1057523045 |
Gnomad | rs1057523045 |
Varsome | rs1057523045 |
LitVar | rs1057523045 |
Map | rs1057523045 |
PheGenI | rs1057523045 |
Biobank | rs1057523045 |
1000 genomes | rs1057523045 |
hgdp | rs1057523045 |
ensembl | rs1057523045 |
geneview | rs1057523045 |
scholar | rs1057523045 |
rs1057523045 | |
pharmgkb | rs1057523045 |
gwascentral | rs1057523045 |
openSNP | rs1057523045 |
23andMe | rs1057523045 |
SNPshot | rs1057523045 |
SNPdbe | rs1057523045 |
MSV3d | rs1057523045 |
GWAS Ctlg | rs1057523045 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057523045(G;G) |
Alt | rs1057523045(G;G) |
Reference | Rs1057523045(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LOC101928076 DSP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.7542271C>G |
CLNSRC | |
CLNACC | RCV000429494.1, |