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 10:87863271 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 7 transcripts and 1 regulatory feature.

Variant displays