Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

About this variant

This variant overlaps 1 transcript and has 2505 individual genotypes.

Variation displays