Original source

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

A/- | Ancestral: A | MAF: 0.01 (-)

Chromosome 16:46669073 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs371496694

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2504 sample genotypes.

Variant displays