Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.08 (G)

Chromosome 16:23362098 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs458121, rs59332118, rs703781

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 1094 individual genotypes.

Variation displays