Original source

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

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

Chromosome 5: between 154474812 and 154474813 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

5:g.154474812_154474813insT

Variation displays