Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.37 (G)
Location

Chromosome 3:122252955 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 3 transcripts, has 1452 individual genotypes and is mentioned in 1 citation.

Variation displays