rs7935346
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7935346(A;A) |
Make rs7935346(A;G) |
Make rs7935346(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 46986828 |
Gene | C11orf49 |
is a | snp |
is | mentioned by |
dbSNP | rs7935346 |
dbSNP (classic) | rs7935346 |
ClinGen | rs7935346 |
ebi | rs7935346 |
HLI | rs7935346 |
Exac | rs7935346 |
Gnomad | rs7935346 |
Varsome | rs7935346 |
LitVar | rs7935346 |
Map | rs7935346 |
PheGenI | rs7935346 |
Biobank | rs7935346 |
1000 genomes | rs7935346 |
hgdp | rs7935346 |
ensembl | rs7935346 |
geneview | rs7935346 |
scholar | rs7935346 |
rs7935346 | |
pharmgkb | rs7935346 |
gwascentral | rs7935346 |
openSNP | rs7935346 |
23andMe | rs7935346 |
SNPshot | rs7935346 |
SNPdbe | rs7935346 |
MSV3d | rs7935346 |
GWAS Ctlg | rs7935346 |
GMAF | 0.4679 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
rs7935346 increases susceptibility to Osteoporotic fractures for carriers of the G allele [PMID 18445777]