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: 0.19 (C)
Location

Chromosome 2:85658890 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1061246, rs3202292

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

This variation has assays on 7 chips - click the plus to show

Variation displays