Original source

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

-/A/G | MAF: 0.29 (A)

Chromosome 4: between 120697801 and 120697802 (forward strand) | View in location tab

Most severe consequence
Evidence status


This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 1100 individual genotypes.

Variation displays