Original source

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

A/C | Ancestral: C | Ambiguity code: M | MAF: 0.46 (C)

Chromosome 2:43812736 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs111172443, rs56883360

This variation has 4 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 4038 individual genotypes and is mentioned in 1 citation.

Variation displays