Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.50 (C)
Location

Chromosome 17:73127683 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 9 HGVS names - click the plus to show

Variation displays