rs121912964
From SNPedia
Merged into | rs63750691 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121912964(C;G) |
Make rs121912964(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 37017521 |
Gene | MLH1 |
is a | snp |
is | mentioned by |
dbSNP | rs121912964 |
dbSNP (classic) | rs121912964 |
ClinGen | rs121912964 |
ebi | rs121912964 |
HLI | rs121912964 |
Exac | rs121912964 |
Gnomad | rs121912964 |
Varsome | rs121912964 |
LitVar | rs121912964 |
Map | rs121912964 |
PheGenI | rs121912964 |
Biobank | rs121912964 |
1000 genomes | rs121912964 |
hgdp | rs121912964 |
ensembl | rs121912964 |
geneview | rs121912964 |
scholar | rs121912964 |
rs121912964 | |
pharmgkb | rs121912964 |
gwascentral | rs121912964 |
openSNP | rs121912964 |
23andMe | rs121912964 |
SNPshot | rs121912964 |
SNPdbe | rs121912964 |
MSV3d | rs121912964 |
GWAS Ctlg | rs121912964 |
Status | Merged into rs63750691 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121912964(G;G) |
Alt | rs121912964(G;G) |
Reference | Rs121912964(C;C) |
Significance | Pathogenic |
Disease | Lynch syndrome II |
Variation | info |
Gene | MLH1 |
CLNDBN | Lynch syndrome II |
Reversed | 0 |
HGVS | NC_000003.11:g.37059012C>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | SCV000038914.1, |