Original source

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

Alleles
C/G/T|Ancestral: C|Ambiguity code: B|MAF: < 0.01 (G)
Location

Chromosome 11:1995167 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 36 transcripts and has 2504 sample genotypes.

Variant displays