This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
A/C/G/T | Ancestral: A | Ambiguity code: N
Location

Chromosome 5:147831537 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001342, CM072067

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_093_SPINK1_167790_0005, 4543, 4542

This variation has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and is associated with 4 phenotypes.

Variation displays