rs35095275
From SNPedia
Merged into | rs421016 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 6 | risk allele, but prone to genotyping confusion |
(A;G) | 3 | carrier for parkinson's risk? |
(G;G) | 0 | most common; unaffected |
Reference | GRCh37.p2 37.2/134 |
Chromosome | 1 |
Position | 155205043 |
Gene | GBA |
is a | snp |
is | mentioned by |
dbSNP | rs35095275 |
dbSNP (classic) | rs35095275 |
ClinGen | rs35095275 |
ebi | rs35095275 |
HLI | rs35095275 |
Exac | rs35095275 |
Gnomad | rs35095275 |
Varsome | rs35095275 |
LitVar | rs35095275 |
Map | rs35095275 |
PheGenI | rs35095275 |
Biobank | rs35095275 |
1000 genomes | rs35095275 |
hgdp | rs35095275 |
ensembl | rs35095275 |
geneview | rs35095275 |
scholar | rs35095275 |
rs35095275 | |
pharmgkb | rs35095275 |
gwascentral | rs35095275 |
openSNP | rs35095275 |
23andMe | rs35095275 |
SNPshot | rs35095275 |
SNPdbe | rs35095275 |
MSV3d | rs35095275 |
GWAS Ctlg | rs35095275 |
Status | Merged into rs421016 |
Max Magnitude | 6 |
Note: this SNP has been retired and replaced by rs421016, representing the exact same nucleotide position yet on the other strand, possibly with more specific flanking sequence.