Original source

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

Alleles
C/A | Ambiguity code: M | MAF: 0.30 (C)
Location

Chromosome 10:133535722 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 7 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 2980 individual genotypes.

Variation displays