Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: < 0.01 (T)
Location

Chromosome 16:30746407 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 2504 sample genotypes.

Variant displays