Original source

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

Alleles
-/CT | MAF: 0.43 (-)
Location

Chromosome 17: between 61575454 and 61575455 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60243473, rs143875197

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

Variation displays