Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 15:74719514 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

15:g.74719514C>T

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 270 sample genotypes and is mentioned in 1 citation.

Variant displays