Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.17 (T)
Location

Chromosome 6:52425961 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3827792

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2511 individual genotypes.

Variation displays