Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.23 (G)
Location

Chromosome 1:183577338 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60096150, rs35377361

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts and has 2558 sample genotypes.

Variant displays