Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (A)
Location

Chromosome 15:64456160 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59155550

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

This variation has assays on 4 chips - click the plus to show

Variation displays