Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 20:762108 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 270 sample genotypes.

Variant displays