Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2504 sample genotypes.

Variant displays