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 14:88417304 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60969781

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 15 transcripts and has 1 sample genotype.

Variant displays