Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 10:87864656 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and 1 regulatory feature.

Variant displays