Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.27 (G)
Location

Chromosome 10:133536033 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59502658

This variation has 7 HGVS names - click the plus to show

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

About this variant

This variant overlaps 9 transcripts and has 2463 individual genotypes.

Variation displays