Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.04 (T)
Location

Chromosome 17:42795422 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CS045336

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs58192643

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 11 transcripts and has 2775 sample genotypes.

Variant displays