Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.43 (G)
Location

Chromosome 6:143946046 (forward strand) | View in location tab

Co-located

with dbSNP rs68014771 (G/A/GG/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs28627035, rs11414469

This variant has 17 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 19 transcripts and has 2509 sample genotypes.

Variant displays