Original source

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

Alleles
-/T
Location

Chromosome 6: between 34426493 and 34426494 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs372724412

HGVS name

6:g.34426493_34426494insT

Variation displays