Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 5:147828022 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM016009

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB SPINK1_194G_A_061411

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 3 transcripts, is associated with 1 phenotype and is mentioned in 6 citations.

Variation displays