Original source

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

Alleles
A/C/G|Ancestral: A|Ambiguity code: V|MAF: 0.04 (G)
Location

Chromosome 6:160707855 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs1652509

HGVS names

This variant has 26 HGVS names - Show

About this variant

This variant overlaps 22 transcripts and has 2505 sample genotypes.

Variant displays