Original source

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

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

Chromosome 8:22164010 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM093904, CM024532, CM022460

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_053_SFTPC_178620_0004, 5083

This variation has 9 HGVS names - click the plus to show

Variation displays