Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 9:139577687 (forward strand) | View in location tab

Co-located

with dbSNP rs374106736 (G/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61595823

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni5

Variation displays