Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B | MAF: < 0.01 (G)
Location

Chromosome 17:61559066 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000017.9:g.58912798C>T

This variation has 18 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays