Original source

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

Alleles
TGAC/-|MAF: 0.12 (-)
Location

Chromosome 6:32635409-32635412 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs147842905

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2508 sample genotypes.

Variant displays