Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.09 (T)
Location

Chromosome 2:210289901 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.210289901C>T

About this variant

This variant overlaps 4 transcripts and has 3028 individual genotypes.

Variation displays