Original source

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

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

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

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

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