Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.46 (C)

Chromosome 16:89737354 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58084694, rs17233840

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 23 transcripts and has 2586 sample genotypes.

Variant displays