Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W
Location

Chromosome 6:160701133 (forward strand) | View in location tab

Most severe consequence
HGVS name

6:g.160701133A>T

About this variant

This variant overlaps 10 transcripts.

Variation displays