Original source

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

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

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

Co-located variant

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