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 10:100989154 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012072, CM085294

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_065_PEO1_606075_0005, 13529

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

Variation displays