Original source

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


Chromosome 1: between 183555503 and 183555504 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs140052983, rs34919085

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 40 individual genotypes.

Variation displays