Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.08 (G)
Location

Chromosome 12:6534437 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 20 transcripts, 1 regulatory feature, has 2506 sample genotypes and is mentioned in 1 citation.

Variant displays