Original source

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

A/- | Ancestral: A

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 87 individual genotypes.

Variation displays