Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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