Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.35 (C)
Location

Chromosome 19:50693133 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58503611

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

19:g.50693133T>C
ENST00000598205.1:c.-4+1569T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays