Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.18 (T)
Location

Chromosome 5:135031908 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2528 sample genotypes and is mentioned in 4 citations.

Variant displays