Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 variant

HGMD-PUBLIC CR057602

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59007920

HGVS name

5:g.157059580T>C

About this variant

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

Variant displays