Original source

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

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.31 (G)

Chromosome 4:1010000 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs5007717

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

Genotyping chips

This variation has assays on: Illumina_Human660W-quad

About this variant

This variant overlaps 8 transcripts and has 1102 individual genotypes.

Variation displays