Original source

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

Alleles
G/T | Ambiguity code: K
Location

Chromosome 19:950264 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1617907, rs8105327, rs350126

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature and has 4 sample genotypes.

Variant displays