Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

About this variant

This variant overlaps 3 transcripts and has 2507 individual genotypes.

Variation displays