Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 19:42085838 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
HGVS name

19:g.42085838G>A

About this variant

This variant overlaps 9 transcripts.

Variant displays