Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.11 (A)
Location

Chromosome 11:34915273 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2504 sample genotypes.

Variant displays