Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.32 (C)
Location

Chromosome 5:150115690 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs58663565

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 3685 sample genotypes and is mentioned in 1 citation.

Variant displays