rs121912972
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121912972(-;-) |
Make rs121912972(-;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 174725004 |
Gene | MSX2 |
is a | snp |
is | mentioned by |
dbSNP | rs121912972 |
dbSNP (classic) | rs121912972 |
ClinGen | rs121912972 |
ebi | rs121912972 |
HLI | rs121912972 |
Exac | rs121912972 |
Gnomad | rs121912972 |
Varsome | rs121912972 |
LitVar | rs121912972 |
Map | rs121912972 |
PheGenI | rs121912972 |
Biobank | rs121912972 |
1000 genomes | rs121912972 |
hgdp | rs121912972 |
ensembl | rs121912972 |
geneview | rs121912972 |
scholar | rs121912972 |
rs121912972 | |
pharmgkb | rs121912972 |
gwascentral | rs121912972 |
openSNP | rs121912972 |
23andMe | rs121912972 |
SNPshot | rs121912972 |
SNPdbe | rs121912972 |
MSV3d | rs121912972 |
GWAS Ctlg | rs121912972 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121912972(-;-) |
Alt | rs121912972(-;-) |
Reference | Rs121912972(G;G) |
Significance | Pathogenic |
Disease | Parietal foramina 1 |
Variation | info |
Gene | MSX2 |
CLNDBN | Parietal foramina 1 |
Reversed | 0 |
HGVS | NC_000005.9:g.174152007delG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000018479.25, |