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
G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: < 0.01 (A)
Location

Chromosome 5:147828053 (forward strand) | View in location tab

Co-located

with COSMIC COSM223032 (G/A) ; HGMD-PUBLIC CM014100

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB SPINK1_163C_T_081111

This variation has 18 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts, has 2504 individual genotypes, is associated with 1 phenotype and is mentioned in 6 citations.

Variation displays