Original source

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

Alleles
GTT/- | MAF: 0.09 (-)
Location

Chromosome 15:41014728-41014730 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs374610247

This variation has 8 HGVS names - click the plus to show

Variation displays