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 6:15627391 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM032218

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14686, NM_032122.3:c.307C>T, 2010_April_001_042_DTNBP1_607145_0001

This variation has 16 HGVS names - click the plus to show

Variation displays