Original source

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

Alleles
-/T | MAF: 0.01 (T)
Location

Chromosome 5: between 153854372 and 153854373 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

5:g.153854372_153854373insT

Variation displays