Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 5:136046407 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CP05317, CM981909, CM971472

Most severe consequence
Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 16 HGVS names - click the plus to show

Variation displays