Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 17:7669118 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs1042533, rs2543551, rs1794290

HGVS names

This variant has 35 HGVS names - Show

About this variant

This variant overlaps 36 transcripts, has 37 sample genotypes and is mentioned in 2 citations.

Variant displays