Original source

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

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 2505 sample genotypes.

Variant displays