Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B | MAF: < 0.01 (T)
Location

Chromosome 8:94249065 (forward strand) | View in location tab

Most severe consequence

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

About this variant

This variant overlaps 4 transcripts and has 2504 individual genotypes.

Variation displays