Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
TGGCAGTAAGCTAAATTCTGTTGGAACATCCATGGAAATTGCCAG/-
Location

Chromosome 8:118947213-118947257 (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.

Variation displays