Original source

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

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

Chromosome 9:95150056 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930240 ; PhenCode FANCC:c.553C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 6270

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays