Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.29 (T)
Location

Chromosome 1:145927267 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

Clinical significance

This variation has 19 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

Variation displays