Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.44 (G)
Location

Chromosome 19:41349610 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 1152 individual genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays