Original source

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

G/T | Ambiguity code: K

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs1617907, rs8105327, rs350126

HGVS names

This variant has 4 HGVS names - Show

About this variant

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

Variant displays