Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 11:27716416 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts.

Variant displays