Original source

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

Alleles
C/G/T|Ancestral: C|Ambiguity code: B
Location

Chromosome 11:1995871 (forward strand)|View in location tab

Most severe consequence
 
Splice region variant
Evidence status

HGVS names

This variant has 28 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 36 transcripts.

Variant displays