Original source

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

Alleles
A/C/T|Ancestral: A|Ambiguity code: H|MAF: 0.08 (T)
Location

Chromosome 6:32635457 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs117534704

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2504 sample genotypes.

Variant displays