Original source

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

A/- | Ancestral: A | MAF: 0.34 (A)

Chromosome 1:113865422 (forward strand) | View in location tab

Most severe consequence
Evidence status


This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 1097 individual genotypes.

Variation displays