Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.17 (G)

Chromosome 13:113315829 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs74242211

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 1094 individual genotypes.

Variation displays