Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.10 (G)
Location

Chromosome 2:47790942 (forward strand) | View in location tab

Co-located

with PhenCode MMR_c.276A>G (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 8 synonyms - click the plus to show

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

This variation has assays on 5 chips - click the plus to show

Variation displays