Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 19:14091875 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs11541566, rs16979459

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays