Original source

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

Alleles
A/- | Ancestral: A | MAF: 0.18 (-)
Location

Chromosome 5:135032674 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 2504 individual genotypes.

Variation displays