Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.38 (A)
Location

Chromosome 14:100824126 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 16 transcripts, has 1368 individual genotypes and is mentioned in 1 citation.

Variation displays