Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A/C|Ancestral: G|Ambiguity code: V|MAF: < 0.01 (A)
Location

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

Co-located variants

COSMIC COSM223032 ; HGMD-PUBLIC CM014100

Most severe consequence
 
Missense variant
Evidence status

Synonyms

LSDB SPINK1_163C_T_081111

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

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

Variant displays