Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)
Location

Chromosome 2:238244921 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM050237 ; PhenCode COL6A3:c.8822C>T (G/A)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 17 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni2.5

Variation displays