Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.21 (G)
Location

Chromosome 3:122284922 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM044584 ; PhenCode CASRdb_c.2968A>G (A/G)

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

Variation displays