Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.37 (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 9 transcripts and has 2512 sample genotypes.

Variant displays