Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
-/C | MAF: 0.02 (C)
Location

Chromosome 11: between 45929391 and 45929392 (forward strand) | View in location tab

Most severe consequence

 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]

This variation has 2 HGVS names - click the plus to show

Variation displays