Original source

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

Alleles
T/-/TT | Ancestral: T
Location

Chromosome 1:17003667 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 20 HGVS names - click the plus to show

Variation displays