Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 5:147211100 (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 10 HGVS names - click the plus to show

Variation displays