Original source

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


Chromosome 1: between 219929525 and 219929526 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs34409360, rs71949445

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2 individual genotypes.

Variation displays