Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 11:17463457 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM991161

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000352.3:c.560T>A, 9256

This variation has 8 HGVS names - click the plus to show

Variation displays