Original source

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

Alleles
A/T|Ambiguity code: W|MAF: 0.03 (T)
Location

Chromosome 6:32643331 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms
HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2505 sample genotypes.

Variant displays