Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.40 (C)
Location

Chromosome 11:68343621 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 2779 sample genotypes and is mentioned in 2 citations.

Variant displays