Original source

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

Alleles
C/G|Ancestral: G|Ambiguity code: S|MAF: 0.05 (G)
Location

Chromosome 17:63918647 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2766 sample genotypes and is mentioned in 2 citations.

Variant displays