Original source

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

Alleles
-/GGTGGGTGTGGT|MAF: 0.41 (GGTGGGTGTGGT)
Location

Chromosome 7: between 151562820 and 151562821 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2504 sample genotypes.

Variant displays