Original source

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

Alleles
-/T
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs140835190, rs71179078

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2 sample genotypes.

Variant displays