rs1057518234
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TTGA;TTGA) | 0 | common in clinvar |
Make rs1057518234(-;-) |
Make rs1057518234(-;TTGA) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 20 |
Position | 5954632 |
Gene | MCM8 |
is a | snp |
is | mentioned by |
dbSNP | rs1057518234 |
dbSNP (classic) | rs1057518234 |
ClinGen | rs1057518234 |
ebi | rs1057518234 |
HLI | rs1057518234 |
Exac | rs1057518234 |
Gnomad | rs1057518234 |
Varsome | rs1057518234 |
LitVar | rs1057518234 |
Map | rs1057518234 |
PheGenI | rs1057518234 |
Biobank | rs1057518234 |
1000 genomes | rs1057518234 |
hgdp | rs1057518234 |
ensembl | rs1057518234 |
geneview | rs1057518234 |
scholar | rs1057518234 |
rs1057518234 | |
pharmgkb | rs1057518234 |
gwascentral | rs1057518234 |
openSNP | rs1057518234 |
23andMe | rs1057518234 |
SNPshot | rs1057518234 |
SNPdbe | rs1057518234 |
MSV3d | rs1057518234 |
GWAS Ctlg | rs1057518234 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057518234(-;-) |
Alt | rs1057518234(-;-) |
Reference | Rs1057518234(TTGA;TTGA) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MCM8 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.5935278_5935281delTTGA |
CLNSRC | |
CLNACC | RCV000414339.1, |