Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.37 (A)

Chromosome 3:58427935 (forward strand) | View in location tab

Most severe consequence
Evidence status


This variation has 16 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 40 transcripts and has 1107 individual genotypes.

Variation displays