Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.18 (G)
Location

Chromosome 1:153561422 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

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

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 3706 sample genotypes and is mentioned in 1 citation.

Variant displays