Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 15:64156761 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 94 individual genotypes and is associated with 1 phenotype.

Variation displays