Original source

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

Alleles
T/-/TTT | Ancestral: T
Location

Chromosome 2:5694667 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 1 individual genotype.

Variation displays