Original source

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

T/- | Ancestral: T

Chromosome 1:237589784 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance


This variant has 5 synonyms - Show

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, has 5 sample genotypes and is associated with 2 phenotypes.

Variant displays