Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.39 (T)
Location

Chromosome 11:8089993 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57969751

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2546 sample genotypes and is mentioned in 5 citations.

Variant displays