Original source

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

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

Chromosome 4:174491347-174491350 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs140833916

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 2550 individual genotypes.

Variation displays