Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: < 0.01 (G)
Location

Chromosome 9:136683235 (forward strand)|View in location tab

Co-located variant

dbSNP rs767279642 (G/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61595823

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 2507 sample genotypes.

Variant displays