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

Co-located

with HGMD-PUBLIC CM992901

Most severe consequence
Evidence status

Clinical significance

Synonyms

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

Variation displays