Original source

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

G/T | Ancestral: G | Ambiguity code: K

Chromosome 3:51979465 (forward strand) | View in location tab


with dbSNP rs201299862 (G/-)

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 21 transcripts and has 1 sample genotype.

Variant displays