rs4987188
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs4987188(A;A) |
| Make rs4987188(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 47416318 |
| Gene | MSH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4987188 |
| dbSNP (classic) | rs4987188 |
| ClinGen | rs4987188 |
| ebi | rs4987188 |
| HLI | rs4987188 |
| Exac | rs4987188 |
| Gnomad | rs4987188 |
| Varsome | rs4987188 |
| LitVar | rs4987188 |
| Map | rs4987188 |
| PheGenI | rs4987188 |
| Biobank | rs4987188 |
| 1000 genomes | rs4987188 |
| hgdp | rs4987188 |
| ensembl | rs4987188 |
| geneview | rs4987188 |
| scholar | rs4987188 |
| rs4987188 | |
| pharmgkb | rs4987188 |
| gwascentral | rs4987188 |
| openSNP | rs4987188 |
| 23andMe | rs4987188 |
| SNPshot | rs4987188 |
| SNPdbe | rs4987188 |
| MSV3d | rs4987188 |
| GWAS Ctlg | rs4987188 |
| GMAF | 0.009183 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs4987188(A;A) rs4987188(T;T) |
| Alt | rs4987188(A;A) rs4987188(T;T) |
| Reference | Rs4987188(G;G) |
| Significance | Non-pathogenic |
| Disease | MSH2 POLYMORPHISM Lynch syndrome not provided not specified Lynch syndrome I Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | MSH2 |
| CLNDBN | MSH2 POLYMORPHISM Lynch syndrome not provided not specified Lynch syndrome I Hereditary cancer-predisposing syndrome |
| Reversed | 0 |
| HGVS | NC_000002.11:g.47643457G>A; NC_000002.11:g.47643457G>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000001832.2, RCV000030257.6, RCV000034561.3, RCV000121567.3, RCV000144615.1, RCV000157760.5, RCV000131668.3, RCV000203979.1, RCV000410421.1, RCV000482522.1, |
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