Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.10 (G)
Location

Chromosome 1:109566417 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60932128

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

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 3687 sample genotypes.

Variant displays