Original source

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

Alleles
AATAACGAGGTCTCTCTC/-
Location

Chromosome 9:125425294-125425311 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs34747081

HGVS name

9:g.125425294_125425311delAATAACGAGGTCTCTCTC

Variation displays