Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.41 (C)
Location

Chromosome 15:46593911 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61705220, rs1711619

HGVS name

15:g.46593911C>T

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays