Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S
Location

Chromosome 11:47438005 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature and has 3 sample genotypes.

Variant displays