Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 10:100989285 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012074

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_063_PEO1_606075_0003, 13527

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

Variation displays