Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.05 (C)
Location

Chromosome 7:128589000 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

7:g.128589000T>C
ENST00000249375.4:c.*128T>C
ENST00000465603.1:c.*1153T>C
ENST00000402030.2:c.*128T>C
ENST00000473745.1:c.*128T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_ImmunoChip

Variation displays