Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.04 (A)
Location

Chromosome 9:35076755 (forward strand) | View in location tab

Co-located

with COSMIC COSM150601 (G/A) ; HGMD-PUBLIC CM015016 ; PhenCode FANCG:c.890C>T (G/A)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

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

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

Variation displays