Original source

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

Alleles
C/G|Ambiguity code: S
Location

Chromosome 20:63919816 (forward strand)|View in location tab

Most severe consequence
 
Mature miRNA variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 8 transcripts, has 2 sample genotypes and is mentioned in 1 citation.

Variant displays