Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.17 (C)
Location

Chromosome 2:47795976 (forward strand) | View in location tab

Co-located

with PhenCode MMR_c.540T>C (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 16 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

Variation displays