Original source

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

Alleles
ATTT/- | MAF: 0.49 (-)
Location

Chromosome 12:20986670-20986673 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs151047605

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

Variation displays