Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.41 (A)
Location

Chromosome 8:128428638 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM073275 ; dbSNP rs75641460 (A/G)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays