Original source

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

Alleles
-/C | MAF: < 0.01 (C)
Location

Chromosome 15: between 66384940 and 66384941 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2504 sample genotypes.

Variant displays