rs121912988
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs121912988(G;G) |
Make rs121912988(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 87610924 |
Gene | DSPP |
is a | snp |
is | mentioned by |
dbSNP | rs121912988 |
dbSNP (classic) | rs121912988 |
ClinGen | rs121912988 |
ebi | rs121912988 |
HLI | rs121912988 |
Exac | rs121912988 |
Gnomad | rs121912988 |
Varsome | rs121912988 |
LitVar | rs121912988 |
Map | rs121912988 |
PheGenI | rs121912988 |
Biobank | rs121912988 |
1000 genomes | rs121912988 |
hgdp | rs121912988 |
ensembl | rs121912988 |
geneview | rs121912988 |
scholar | rs121912988 |
rs121912988 | |
pharmgkb | rs121912988 |
gwascentral | rs121912988 |
openSNP | rs121912988 |
23andMe | rs121912988 |
SNPshot | rs121912988 |
SNPdbe | rs121912988 |
MSV3d | rs121912988 |
GWAS Ctlg | rs121912988 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121912988(G;G) |
Alt | rs121912988(G;G) |
Reference | Rs121912988(T;T) |
Significance | Pathogenic |
Disease | Denticles |
Variation | info |
Gene | DSPP |
CLNDBN | Denticles |
Reversed | 0 |
HGVS | NC_000004.11:g.88532076T>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000018353.27, |