Original source

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

Alleles
-/A/G | MAF: 0.29 (A)
Location

Chromosome 4: between 121618956 and 121618957 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 14 HGVS names - click the plus to show

Variation displays