Original source

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

-/A/C | MAF: 0.17 (C)

Chromosome 12: between 21131693 and 21131694 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs143871795

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

About this variant

This variant overlaps 12 transcripts and has 1092 individual genotypes.

Variation displays