Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/- | Ancestral: T
Location

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

Most severe consequence
Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts.

Variation displays