Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome 16:30719330 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs6565200, rs59720307

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

About this variant

This variant overlaps 4 transcripts and has 2510 individual genotypes.

Variation displays