Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (T)
Location

Chromosome 4:56393690 (forward strand) | View in location tab

Co-located

with dbSNP rs41530949 (C/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59684593

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

Variation displays