Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
CCTGGGGGGTCTTCTAACTACTGG/-
Location

Chromosome 1:110145759-110145782 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.110145759_110145782delCCTGGGGGGTCTTCTAACTACTGG

Variation displays