Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.04 (G)
Location

Chromosome 6:154076193 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 18 transcripts, has 2788 sample genotypes and is mentioned in 1 citation.

Variant displays