Original source

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

Alleles
A/G|Ambiguity code: R|MAF: 0.49 (G)
Location

Chromosome 11:2312445 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59656042

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 17 transcripts, 1 regulatory feature, has 3690 sample genotypes and is mentioned in 1 citation.

Variant displays