Original source

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

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

Chromosome 10:119662226 (forward strand) | View in location tab

Co-located

with dbSNP rs150785296 (G/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61202285

This variation has 5 HGVS names - click the plus to show

Variation displays