Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.20 (T)
Location

Chromosome 11:34466548 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57958064, rs17881806

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2555 sample genotypes.

Variant displays