Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 16:79627675 (forward strand) | View in location tab

Co-located

with dbSNP rs79761316 (T/A)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs35268223

This variation has 2 HGVS names - click the plus to show

Variation displays