Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2668 sample genotypes and is mentioned in 4 citations.

Variant displays