Original source

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

Alleles
CCGCGC/- | MAF: 0.36 (CCGCGC)
Location

Chromosome 5:135028717-135028722 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs145747214

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

About this variant

This variant overlaps 10 transcripts and has 2504 individual genotypes.

Variation displays