Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/GTGTGTGTGTGTGTGT | MAF: 0.21 (GTGTGTGTGTGTGTGT)
Location

Chromosome 12: between 117208391 and 117208392 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2505 individual genotypes.

Variation displays