rs876661222
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs876661222(-;ATTA) |
Make rs876661222(ATTA;ATTA) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 47806313 |
Gene | MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs876661222 |
dbSNP (classic) | rs876661222 |
ClinGen | rs876661222 |
ebi | rs876661222 |
HLI | rs876661222 |
Exac | rs876661222 |
Gnomad | rs876661222 |
Varsome | rs876661222 |
LitVar | rs876661222 |
Map | rs876661222 |
PheGenI | rs876661222 |
Biobank | rs876661222 |
1000 genomes | rs876661222 |
hgdp | rs876661222 |
ensembl | rs876661222 |
geneview | rs876661222 |
scholar | rs876661222 |
rs876661222 | |
pharmgkb | rs876661222 |
gwascentral | rs876661222 |
openSNP | rs876661222 |
23andMe | rs876661222 |
SNPshot | rs876661222 |
SNPdbe | rs876661222 |
MSV3d | rs876661222 |
GWAS Ctlg | rs876661222 |
Merged from | Rs754183111 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876661222(ATTA;ATTA) |
Alt | rs876661222(ATTA;ATTA) |
Reference | Rs876661222(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MSH6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.48033449_48033452dupATTA |
CLNSRC | |
CLNACC | RCV000216513.1, |