Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.32 (A)
Location

Chromosome 6:160753106 (forward strand)|View in location tab

Co-located variant

dbSNP rs57037765 (A/G)

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2545 sample genotypes.

Variant displays