rs1064795264
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GAGCGCGGCC;GAGCGCGGCC) | 0 | common in clinvar |
Chromosome | 2 |
Position | 47403230 |
Gene | MSH2 |
is a | snp |
is | mentioned by |
dbSNP | rs1064795264 |
dbSNP (classic) | rs1064795264 |
ClinGen | rs1064795264 |
ebi | rs1064795264 |
HLI | rs1064795264 |
Exac | rs1064795264 |
Gnomad | rs1064795264 |
Varsome | rs1064795264 |
LitVar | rs1064795264 |
Map | rs1064795264 |
PheGenI | rs1064795264 |
Biobank | rs1064795264 |
1000 genomes | rs1064795264 |
hgdp | rs1064795264 |
ensembl | rs1064795264 |
geneview | rs1064795264 |
scholar | rs1064795264 |
rs1064795264 | |
pharmgkb | rs1064795264 |
gwascentral | rs1064795264 |
openSNP | rs1064795264 |
23andMe | rs1064795264 |
SNPshot | rs1064795264 |
SNPdbe | rs1064795264 |
MSV3d | rs1064795264 |
GWAS Ctlg | rs1064795264 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064795264(-;-) |
Alt | rs1064795264(-;-) |
Reference | Rs1064795264(GAGCGCGGCC;GAGCGCGGCC) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MSH2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.47630369_47630378delCGCGGCCGAG |
CLNSRC | |
CLNACC | RCV000486490.1, |