Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.13 (T)
Location

Chromosome 2:231508099 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

2:g.231508099C>T

About this variant

This variant overlaps 1 transcript and has 2504 sample genotypes.

Variant displays