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 17:15260663 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM044031 ; PhenCode IPNMDB_751 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000304.2:c.65C>T, 9900, 2010_April_001_189_PMP22_601097_0019

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

Variation displays