Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.01 (T)
Location

Chromosome 10:71962849 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

10:g.71962849C>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 2504 sample genotypes.

Variant displays