Original source

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

Alleles
T/-|Ancestral: T
Location

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

Co-located variant

dbSNP rs377184807 (T/G)

Most severe consequence
 
Frameshift variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript.

Variant displays