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 18:51048790 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB SCV000042345

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts, has 1092 individual genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variation displays