Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.03 (A)
Location

Chromosome 10:48399707 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61045810

This variant has 7 HGVS names - click the plus to show

This variant has assays on 8 chips - click the plus to show

About this variant

Variant displays