Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.04 (A)
Location

Chromosome 17:50199874 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2082 individual genotypes and is mentioned in 1 citation.

Variation displays