Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.26 (T)
Location

Chromosome 19:15465232 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58346433

HGVS name

19:g.15465232T>C

About this variant

This variant overlaps 4 transcripts and has 2510 individual genotypes.

Variation displays