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
Location

Chromosome 17:43124044 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012906, CM004187

Most severe consequence
Clinical significance

Synonyms

LSDB U14680.1:c.53T>A, U14680.1:c.53T>C

This variation has 84 HGVS names - click the plus to show

Variation displays