Original source

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

Alleles
TTTG/- | MAF: 0.50 (-)
Location

Chromosome 18:5422460-5422463 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 2510 individual genotypes.

Variation displays