Original source

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

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

Chromosome 13:27920364 (forward strand) | View in location tab


with HGMD-PUBLIC CM992901

Most severe consequence
Evidence status

Clinical significance


LSDB 9483, IPF1_226G_A_072211

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 2 transcripts, is associated with 3 phenotypes and is mentioned in 5 citations.

Variation displays