Original source

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

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

Chromosome 6:111085887 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

6:g.111085887C>T

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays