Original source

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

Alleles
GTTT/-
Location

Chromosome 18:5422463-5422466 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs144266715

This variation has 11 HGVS names - click the plus to show

Variation displays