rs7006527
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7006527(A;A) |
Make rs7006527(A;C) |
Make rs7006527(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 100012277 |
Gene | RGS22 |
is a | snp |
is | mentioned by |
dbSNP | rs7006527 |
dbSNP (classic) | rs7006527 |
ClinGen | rs7006527 |
ebi | rs7006527 |
HLI | rs7006527 |
Exac | rs7006527 |
Gnomad | rs7006527 |
Varsome | rs7006527 |
LitVar | rs7006527 |
Map | rs7006527 |
PheGenI | rs7006527 |
Biobank | rs7006527 |
1000 genomes | rs7006527 |
hgdp | rs7006527 |
ensembl | rs7006527 |
geneview | rs7006527 |
scholar | rs7006527 |
rs7006527 | |
pharmgkb | rs7006527 |
gwascentral | rs7006527 |
openSNP | rs7006527 |
23andMe | rs7006527 |
SNPshot | rs7006527 |
SNPdbe | rs7006527 |
MSV3d | rs7006527 |
GWAS Ctlg | rs7006527 |
GMAF | 0.1653 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 24403052] Germline Sequence Variants in TGM3 and RGS22 Confer Risk of Basal Cell Carcinoma