Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 3:63862669 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 38 individual genotypes.

Variation displays