Original source

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


Chromosome 12: between 20832950 and 20832951 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs149223350

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 8 individual genotypes.

Variation displays