Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.45 (A)

Chromosome 5:134528909 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs649399, rs57683373

This variation has 8 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2563 individual genotypes.

Variation displays