Original source

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

Alleles
-/CTTT
Location

Chromosome 11: between 113346856 and 113346857 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs138644106

HGVS name

11:g.113346856_113346857insCTTT

Variation displays