Original source

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

Alleles
TCT/- | MAF: 0.02 (-)
Location

Chromosome 12:43757178-43757180 (forward strand) | View in location tab

Co-located

with dbSNP rs199759992 (TCT/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs72656909, rs144702200

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

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

Variation displays