Original source

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

Alleles
TTTCT/- | MAF: 0.39 (-)
Location

Chromosome 19:49478172-49478176 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

Variation displays