Original source

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

T/- | Ancestral: T

Chromosome 14:30877808 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and is associated with 1 phenotype.

Variant displays