Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 10:68989082 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM051942

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_045_KIAA1279_609367_0002, 16292

This variation has 3 HGVS names - click the plus to show

Variation displays