| All of dbSNP (then use filters on results page) |
all[sb]
|
| dbSNP RefSNP ID |
Single: 328; Multiple 328,226,200
|
| Gene |
Gene symbol PTEN[Gene Name] or gene ID 4023[Gene_ID]
|
| Genomic location of a single position or range on GRCh38. See the announcement and the guide for using GRCh37 coordinates |
6[Chromosome] AND (1500000:3000000[Base Position] )
|
| Clinical significance |
"pathogenic"[Clinical Significance]) OR "likely pathogenic"[Clinical Significance]
|
Global or study-wide minor allele frequency (GMAF) of a single frequency or range
(Note the required zero padding frequency as shown in example for 0.001 and 0.01) |
00000.0010:00000.0100[GLOBAL_MAF]
|