Original source

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

Alleles
T/C|Ambiguity code: Y|MAF: 0.50 (C)
Location

Chromosome 11:18397885 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 21 HGVS names - Show

About this variant

This variant overlaps 25 transcripts and has 2580 sample genotypes.

Variant displays