Original source

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

Alleles
TT/-
Location

Chromosome 10:102229842-102229843 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.102229842_102229843delTT

Variation displays