Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | 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

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

Most severe consequence
Evidence status

Synonyms

LSDB SPINK1_163C_T_081111

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni5, Illumina_1M-duo

Variation displays