Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.37 (T)
Location

Chromosome 5:157059580 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR057602

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59007920

HGVS name

5:g.157059580T>C

About this variant

This variant overlaps 5 transcripts, has 2510 individual genotypes and is mentioned in 1 citation.

Variation displays