Original source

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

-/A | MAF: 0.17 (-)

Chromosome 16: between 46675010 and 46675011 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2514 sample genotypes.

Variant displays