This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
A/C/G/T | Ancestral: G | Ambiguity code: N | 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

This variant has 12 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 21 transcripts, 1 regulatory feature, has 3756 sample genotypes and is mentioned in 3 citations.

Variant displays