Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.11 (C)
Location

Chromosome 11:34440118 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17881625

This variant has 2 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2555 sample genotypes and is mentioned in 1 citation.

Variant displays