Original source

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

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.20 (A)

Chromosome 1:7963528 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs520152

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 1105 individual genotypes.

Variation displays