rs6697953
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6697953(C;C) |
Make rs6697953(C;T) |
Make rs6697953(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 241291207 |
Gene | RGS7 |
is a | snp |
is | mentioned by |
dbSNP | rs6697953 |
dbSNP (classic) | rs6697953 |
ClinGen | rs6697953 |
ebi | rs6697953 |
HLI | rs6697953 |
Exac | rs6697953 |
Gnomad | rs6697953 |
Varsome | rs6697953 |
LitVar | rs6697953 |
Map | rs6697953 |
PheGenI | rs6697953 |
Biobank | rs6697953 |
1000 genomes | rs6697953 |
hgdp | rs6697953 |
ensembl | rs6697953 |
geneview | rs6697953 |
scholar | rs6697953 |
rs6697953 | |
pharmgkb | rs6697953 |
gwascentral | rs6697953 |
openSNP | rs6697953 |
23andMe | rs6697953 |
SNPshot | rs6697953 |
SNPdbe | rs6697953 |
MSV3d | rs6697953 |
GWAS Ctlg | rs6697953 |
GMAF | 0.2681 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.[PMID 19626040]