Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.41 (C)
Location

Chromosome 11:6389167 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61671586

HGVS name

11:g.6389167T>C

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 10 transcripts and has 3693 sample genotypes.

Variant displays