Original source

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

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

Chromosome 1:12165288 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.12165288T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts, has 1377 individual genotypes and is mentioned in 1 citation.

Variation displays