Original source

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

Alleles
T/A/C | Ancestral: T | Ambiguity code: H | MAF: 0.03 (A)
Location

Chromosome 13:48234436 (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 5 transcripts and has 2505 individual genotypes.

Variation displays