Original source

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

Alleles
-/A | MAF: 0.37 (A)
Location

Chromosome 2: between 127285982 and 127285983 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 8 transcripts and has 2510 individual genotypes.

Variation displays