Original source

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


Chromosome 19: between 33387007 and 33387008 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs35012994

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

About this variant

This variant overlaps 18 transcripts and has 4 individual genotypes.

Variation displays