Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 19:45864643 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59351438

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 2514 individual genotypes.

Variation displays