Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.22 (G)
Location

Chromosome 9:712156 (forward strand) | View in location tab

Co-located

with COSMIC COSM150570 (T/G)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

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

Variation displays