Original source

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

-/AC | MAF: 0.11 (-)

Chromosome 5: between 135028467 and 135028468 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs111997779, rs142537552

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2507 individual genotypes.

Variation displays