Original source

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

Alleles
AATAACGAGGTCTCTCTC/-
Location

Chromosome 9:122663015-122663032 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs34747081

HGVS name

9:g.122663015_122663032delAATAACGAGGTCTCTCTC

About this variant

This variant overlaps 2 transcripts.

Variation displays