rs577721086
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common genotype |
Make rs577721086(C;C) |
Make rs577721086(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 127118902 |
Gene | LOC105377989, RSPO3 |
is a | snp |
is | mentioned by |
dbSNP | rs577721086 |
dbSNP (classic) | rs577721086 |
ClinGen | rs577721086 |
ebi | rs577721086 |
HLI | rs577721086 |
Exac | rs577721086 |
Gnomad | rs577721086 |
Varsome | rs577721086 |
LitVar | rs577721086 |
Map | rs577721086 |
PheGenI | rs577721086 |
Biobank | rs577721086 |
1000 genomes | rs577721086 |
hgdp | rs577721086 |
ensembl | rs577721086 |
geneview | rs577721086 |
scholar | rs577721086 |
rs577721086 | |
pharmgkb | rs577721086 |
gwascentral | rs577721086 |
openSNP | rs577721086 |
23andMe | rs577721086 |
SNPshot | rs577721086 |
SNPdbe | rs577721086 |
MSV3d | rs577721086 |
GWAS Ctlg | rs577721086 |
Max Magnitude | 0 |
[PMID 26733130] Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures.