Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.30 (T)
Location

Chromosome 13:27790883 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1745478, rs57703655

HGVS name

13:g.27790883T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays