Original source

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

Alleles
-/T
Location

Chromosome 19: between 49063013 and 49063014 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs140835190, rs71179078

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 2 individual genotypes.

Variation displays