Original source

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

Alleles
-/CTTT
Location

Chromosome 11: between 113476134 and 113476135 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs138644106

HGVS name

11:g.113476134_113476135insCTTT

Variation displays