Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

G/A|Ancestral: G|Ambiguity code: R|MAF: 0.05 (A)

Chromosome 9:35076758 (forward strand)|View in location tab

Co-located variants

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

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 14 transcripts, has 4148 sample genotypes and is associated with 1 phenotype.

Variant displays