Original source

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

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, has 2779 sample genotypes and is mentioned in 5 citations.

Variant displays