rs786201007
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs786201007(-;AGGCGGAGCACCCCAAGCC) |
Make rs786201007(AGGCGGAGCACCCCAAGCC;AGGCGGAGCACCCCAAGCC) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 12717916 |
Gene | CDKN1B, GPR19 |
is a | snp |
is | mentioned by |
dbSNP | rs786201007 |
dbSNP (classic) | rs786201007 |
ClinGen | rs786201007 |
ebi | rs786201007 |
HLI | rs786201007 |
Exac | rs786201007 |
Gnomad | rs786201007 |
Varsome | rs786201007 |
LitVar | rs786201007 |
Map | rs786201007 |
PheGenI | rs786201007 |
Biobank | rs786201007 |
1000 genomes | rs786201007 |
hgdp | rs786201007 |
ensembl | rs786201007 |
geneview | rs786201007 |
scholar | rs786201007 |
rs786201007 | |
pharmgkb | rs786201007 |
gwascentral | rs786201007 |
openSNP | rs786201007 |
23andMe | rs786201007 |
SNPshot | rs786201007 |
SNPdbe | rs786201007 |
MSV3d | rs786201007 |
GWAS Ctlg | rs786201007 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786201007(CAGGCGGAGCACCCCAAGC;CAGGCGGAGCACCCCAAGC) |
Alt | rs786201007(CAGGCGGAGCACCCCAAGC;CAGGCGGAGCACCCCAAGC) |
Reference | Rs786201007(-;-) |
Significance | Pathogenic |
Disease | Multiple endocrine neoplasia |
Variation | info |
Gene | LOC101929220 CDKN1B |
CLNDBN | Multiple endocrine neoplasia, type 4 |
Reversed | 0 |
HGVS | NC_000012.11:g.12870832_12870850dup19 |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000162205.4, |