Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 2:236165988 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 5 transcripts and has 29 individual genotypes.

Variation displays