Original source

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

Alleles
T/-/TTTAT | Ancestral: T
Location

Chromosome 11:120262988 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs34863596, rs71470997

This variation has 12 HGVS names - click the plus to show

Variation displays