Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.19 (C)
Location

Chromosome 1:8023726 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1173412, rs835733, rs659776

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays