Original source

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

Alleles
-/AC | MAF: 0.15 (-)
Location

Chromosome 5: between 135028467 and 135028468 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs111997779, rs142537552

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

Variation displays