Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.07 (T)
Location

Chromosome 11:69809714 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs57025302

HGVS name

11:g.69809714C>T

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 1 transcript, has 3613 sample genotypes and is mentioned in 1 citation.

Variant displays