Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: < 0.01 (C)
Location

Chromosome 6:43515540 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 28 transcripts and has 2504 sample genotypes.

Variant displays