Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.12 (C)
Location

Chromosome 15:74035865 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM097806

Most severe consequence
Evidence status

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays