Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.02 (A)
Location

Chromosome 12:6840888 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs2234963

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

About this variant

This variant overlaps 21 transcripts, has 1 sample genotype and is mentioned in 2 citations.

Variant displays