rs35502531
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AA;AA) | 0 | common in clinvar |
Make rs35502531(AA;GC) |
Make rs35502531(GC;GC) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 37047639 |
Gene | MLH1 |
is a | snp |
is | mentioned by |
dbSNP | rs35502531 |
dbSNP (classic) | rs35502531 |
ClinGen | rs35502531 |
ebi | rs35502531 |
HLI | rs35502531 |
Exac | rs35502531 |
Gnomad | rs35502531 |
Varsome | rs35502531 |
LitVar | rs35502531 |
Map | rs35502531 |
PheGenI | rs35502531 |
Biobank | rs35502531 |
1000 genomes | rs35502531 |
hgdp | rs35502531 |
ensembl | rs35502531 |
geneview | rs35502531 |
scholar | rs35502531 |
rs35502531 | |
pharmgkb | rs35502531 |
gwascentral | rs35502531 |
openSNP | rs35502531 |
23andMe | rs35502531 |
SNPshot | rs35502531 |
SNPdbe | rs35502531 |
MSV3d | rs35502531 |
GWAS Ctlg | rs35502531 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs35502531(GC;GC) |
Alt | rs35502531(GC;GC) |
Reference | Rs35502531(AA;AA) |
Significance | Other |
Disease | Lynch syndrome II not provided Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome I |
Variation | info |
Gene | MLH1 |
CLNDBN | Lynch syndrome II not provided Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome I |
Reversed | 0 |
HGVS | NC_000003.11:g.37089130_37089131delAAinsGC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000018620.4, RCV000034542.1, RCV000075382.3, RCV000121363.2, RCV000130907.5, RCV000144600.1, |