Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

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

Co-located

with HGMD-PUBLIC CM992901

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 9483, IPF1_226G_A_072211

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

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 2 transcripts, has 2504 sample genotypes, is associated with 3 phenotypes and is mentioned in 6 citations.

Variant displays