Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.29 (T)
Location

Chromosome 19:1221546 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs60672357, rs3752225

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2838 sample genotypes and is mentioned in 5 citations.

Variant displays