Original source

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

Alleles
A/- | Ancestral: A
Location

Chromosome 17:28401037 (forward strand) | View in location tab

Co-located

with dbSNP rs200023006 (A/G)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs144541722, rs375885116

This variation has 8 HGVS names - click the plus to show

Variation displays