Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome 2:46295660 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2504 sample genotypes.

Variant displays