Original source

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

Alleles
C/- | MAF: 0.41 (-)
Location

Chromosome 2:232539050 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs139006344, rs367681527

HGVS name

2:g.232539050delC

About this variant

This variant overlaps 7 transcripts and has 2507 individual genotypes.

Variation displays