Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.28 (T)
Location

Chromosome 12:132624162 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs1135607, rs3198376

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 19 transcripts, has 3772 sample genotypes and is mentioned in 1 citation.

Variant displays