Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.27 (T)
Location

Chromosome 18:902964 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs61563249

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2767 sample genotypes.

Variant displays