Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.07 (C)
Location

Chromosome 11:102875061 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17296532

HGVS name

11:g.102875061T>C

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays