rs1064793234
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AG;AG) | 0 | common in clinvar |
Chromosome | 7 |
Position | 5987185 |
Gene | PMS2 |
is a | snp |
is | mentioned by |
dbSNP | rs1064793234 |
dbSNP (classic) | rs1064793234 |
ClinGen | rs1064793234 |
ebi | rs1064793234 |
HLI | rs1064793234 |
Exac | rs1064793234 |
Gnomad | rs1064793234 |
Varsome | rs1064793234 |
LitVar | rs1064793234 |
Map | rs1064793234 |
PheGenI | rs1064793234 |
Biobank | rs1064793234 |
1000 genomes | rs1064793234 |
hgdp | rs1064793234 |
ensembl | rs1064793234 |
geneview | rs1064793234 |
scholar | rs1064793234 |
rs1064793234 | |
pharmgkb | rs1064793234 |
gwascentral | rs1064793234 |
openSNP | rs1064793234 |
23andMe | rs1064793234 |
SNPshot | rs1064793234 |
SNPdbe | rs1064793234 |
MSV3d | rs1064793234 |
GWAS Ctlg | rs1064793234 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064793234(-;-) |
Alt | rs1064793234(-;-) |
Reference | Rs1064793234(AG;AG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PMS2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000007.13:g.6026816_6026817delCT |
CLNSRC | |
CLNACC | RCV000482204.1, |