Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.17 (A)
Location

Chromosome 19:5839602 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs17748601, rs57750337

This variant has 5 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 3888 sample genotypes.

Variant displays