Original source

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

A/- | Ancestral: A | MAF: 0.01 (-)

Chromosome 2:189783268 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs369571586, rs140337249

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 23 transcripts and has 2591 individual genotypes.

Variation displays