Original source

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

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

Chromosome 17:15260681 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920585 ; PhenCode IPNMDB_4 (A/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000304.2:c.47T>C, 2010_April_001_177_PMP22_601097_0002, 9883

This variation has 18 HGVS names - click the plus to show

Variation displays