Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/- | Ancestral: C | MAF: < 0.01 (-)

Chromosome 5:175440251 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2504 sample genotypes.

Variant displays