Original source

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

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

Chromosome 12:48104135 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts and has 2504 sample genotypes.

Variant displays