Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 5:41733245 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs140280056

This variation has 7 HGVS names - click the plus to show

Variation displays