Original source

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

Alleles
T/C|Ambiguity code: Y|MAF: 0.36 (T)
Location

Chromosome 11:18403471 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60322231, rs59107852

HGVS names

This variant has 17 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant overlaps 25 transcripts and has 4309 sample genotypes.

Variant displays