Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 9:95101723 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920267 ; PhenCode FANCC:c.1661T>C (A/G)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_000136.2:c.1661T>C_1265077451, 6269

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

Genotyping chips

This variant has assays on: HumanCoreExome-12

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature and is associated with 3 phenotypes.

Variant displays