Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.36 (C)
Location

Chromosome 19:1220322 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, has 2506 sample genotypes and is mentioned in 2 citations.

Variant displays