Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)
Location

Chromosome 15:64160123 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

This variation has 6 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 1570 individual genotypes and is associated with 1 phenotype.

Variation displays