Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.06 (A)
Location

Chromosome 10:27715431 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17683190, rs57922420

This variant has 3 HGVS names - click the plus to show

Genotyping chips

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

About this variant

Variant displays