Original source

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

Alleles
TA/- | MAF: 0.17 (-)
Location

Chromosome 13:23213754-23213755 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs141802795

This variation has 4 HGVS names - click the plus to show

Variation displays