Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 17:42787485 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012649

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10655, NM_032387.4:c.1684G>A

This variation has 6 HGVS names - click the plus to show

Variation displays