Original source

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

Alleles
C/G | Ancestral: T | Ambiguity code: S | MAF: 0.27 (G)
Location

Chromosome 5:157059492 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs62381165

HGVS name

5:g.157059492C>G

About this variant

This variant overlaps 5 transcripts, has 2508 sample genotypes and is mentioned in 2 citations.

Variant displays