Original source

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

Alleles
-/AAT/ATA|MAF: 0.23 (-)
Location

Chromosome 6: between 144037703 and 144037704 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs140506447

HGVS names

This variant has 24 HGVS names - Show

About this variant

This variant overlaps 22 transcripts and has 2510 sample genotypes.

Variant displays