Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.37 (T)
Location

Chromosome 11:2129074 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60735850

HGVS name

11:g.2129074T>C

About this variant

This variant overlaps 10 transcripts and has 2512 sample genotypes.

Variant displays