Original source

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

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

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

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs1042533, rs2543551, rs1794290

This variant has 35 HGVS names - click the plus to show

About this variant

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

Variant displays