Original source

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

C/- | Ancestral: C | MAF: 0.05 (-)

Chromosome 17:4901885 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs377046464, rs144972793

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2505 sample genotypes.

Variant displays