Original source

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

Alleles
TT/-
Location

Chromosome 1:17003667-17003668 (forward strand) | View in location tab

Most severe consequence

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 2 individual genotypes.

Variation displays