Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/G
Location

Chromosome 19: between 51903028 and 51903029 (forward strand) | View in location tab

Most severe consequence

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts.

Variation displays