Original source

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

Alleles
A/G/T | Ancestral: A | Ambiguity code: D | MAF: 0.24 (G)
Location

Chromosome 15:74719300 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR961724

Most severe consequence
Evidence status

Synonyms

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

Variation displays