Original source

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

Alleles
-/AAAGC | MAF: 0.04 (AAAGC)
Location

Chromosome 2: between 237074047 and 237074048 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

Variation displays