Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.29 (T)
Location

Chromosome 2:232537797 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59848052

HGVS name

2:g.232537797C>T

About this variant

This variant overlaps 7 transcripts and has 2508 individual genotypes.

Variation displays