Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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