Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.05 (T)
Location

Chromosome 9:72816160 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11956145

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 2541 individual genotypes.

Variation displays