Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

G/T|Ancestral: T|Ambiguity code: K|MAF: 0.35 (G)

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

Co-located variant

dbSNP rs150785296 (G/-)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61202285

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2507 sample genotypes.

Variant displays