Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.09 (G)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs458121, rs59332118, rs703781

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2506 sample genotypes.

Variant displays