Original source

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

-/C | MAF: 0.29 (-)

Chromosome 18: between 5408276 and 5408277 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs142726137

This variation has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 1096 individual genotypes.

Variation displays