Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.30 (-)
Location

Chromosome 18:5467381 (forward strand) | View in location tab

Co-located

with dbSNP rs562214351 (C/A)

Most severe consequence
Evidence status

This variation has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts and has 2513 individual genotypes.

Variation displays