Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.07 (G)
Location

Chromosome 10:99531546 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.99531546C>G

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 5 transcripts and has 2505 individual genotypes.

Variation displays