Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2573 sample genotypes.

Variant displays