Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/G/T|Ancestral: G|Ambiguity code: D|MAF: 0.38 (G)
Location

Chromosome 17:50185414 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3202282, rs61392997

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 14 transcripts, 1 regulatory feature, has 3756 sample genotypes and is mentioned in 4 citations.

Variant displays