Original source

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

A/G|Ancestral: A|Ambiguity code: R|MAF: 0.34 (A)

Chromosome 2:232542095 (forward strand)|View in location tab

Co-located variant

dbSNP rs200832914 (A/-)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57142893

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2507 sample genotypes.

Variant displays