Original source

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

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

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