Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.32 (T)
Location

Chromosome 11:18026269 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CS034323

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59956346

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 5 transcripts, has 3967 sample genotypes and is mentioned in 58 citations.

Variant displays