Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.04 (G)
Location

Chromosome 11:46054967 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61600990, rs17789587

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

Variation displays