Original source

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

Alleles
-/T | MAF: 0.02 (T)
Location

Chromosome 16: between 88425485 and 88425486 (forward strand) | View in location tab

Most severe consequence
HGVS name

16:g.88425485_88425486insT

Variation displays