Original source

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

Alleles
A/C/G|Ancestral: A|Ambiguity code: V|MAF: < 0.01 (G)
Location

Chromosome 10:87858866 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2504 sample genotypes.

Variant displays