Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.03 (T)
Location

Chromosome 13:113323731 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

13:g.113323731C>T

About this variant

This variant overlaps 7 transcripts and has 2773 sample genotypes.

Variant displays