Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 11:71435530 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 2 synonyms - click the plus to show

This variant has 12 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 8 transcripts, has 2550 sample genotypes and is mentioned in 1 citation.

Variant displays