Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 6:159907647 (forward strand) | View in location tab

Co-located

with dbSNP rs377184807 (T/G)

Most severe consequence

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript.

Variation displays